1:  Brailey LL, Davis T, Kolker SE, Murry TC, Thomas D, Bale AE, Ruhoy SM. 
 Congenital linear unilateral basal cell nevus: a case report with patched gene
molecular studies.
J Cutan Pathol. 2007 Jan;34(1):65-70. 
PMID: 17214858 [PubMed - indexed for MEDLINE]

2:  Cajaiba MM, Bale AE, Alvarez-Franco M, McNamara J, Reyes-Mugica M. 
 Rhabdomyosarcoma, Wilms tumor, and deletion of the patched gene in Gorlin
syndrome.
Nat Clin Pract Oncol. 2006 Oct;3(10):575-80. 
PMID: 17019435 [PubMed - indexed for MEDLINE]

3:  Risch HA, Bale AE, Beck PA, Zheng W. 
 PGR +331 A/G and increased risk of epithelial ovarian cancer.
Cancer Epidemiol Biomarkers Prev. 2006 Sep;15(9):1738-41. 
PMID: 16985038 [PubMed - indexed for MEDLINE]

4:  Pejovic T, Yates JE, Liu HY, Hays LE, Akkari Y, Torimaru Y, Keeble W,
Rathbun RK, Rodgers WH, Bale AE, Ameziane N, Zwaan CM, Errami A, Thuillier P,
Cappuccini F, Olson SB, Cain JM, Bagby GC Jr. 
 Cytogenetic instability in ovarian epithelial cells from women at risk of
ovarian cancer.
Cancer Res. 2006 Sep 15;66(18):9017-25. 
PMID: 16982743 [PubMed - indexed for MEDLINE]

5:  Busygina V, Kottemann MC, Scott KL, Plon SE, Bale AE. 
 Multiple Endocrine Neoplasia Type 1 Interacts with Forkhead Transcription
Factor CHES1 in DNA Damage Response.
Cancer Res. 2006 Sep 1;66(17):8397-403. 
PMID: 16951149 [PubMed - in process]

6:  Klein RD, Thorland EC, Gonzales PR, Beck PA, Dykas DJ, McGrath JM, Bale AE. 
 A multiplex assay for the detection and mapping of complex glycerol kinase
deficiency.
Clin Chem. 2006 Oct;52(10):1864-70. Epub 2006 Aug 3. 
PMID: 16887896 [PubMed - indexed for MEDLINE]

7:  Marek LR, Bale AE. 
 Drosophila homologs of FANCD2 and FANCL function in DNA repair.
DNA Repair (Amst). 2006 Nov 8;5(11):1317-26. Epub 2006 Jul 21. 
PMID: 16860002 [PubMed - indexed for MEDLINE]

8:  Yamaguchi S, Brailey LL, Morizono H, Bale AE, Tuchman M. 
 Mutations and polymorphisms in the human ornithine transcarbamylase (OTC) gene.
Hum Mutat. 2006 Jul;27(7):626-32. 
PMID: 16786505 [PubMed - indexed for MEDLINE]

9:  Klein RD, Dykas DJ, Bale AE. 
 Clinical testing for the nevoid basal cell carcinoma syndrome in a DNA
diagnostic laboratory.
Genet Med. 2005 Nov-Dec;7(9):611-9. 
PMID: 16301862 [PubMed - indexed for MEDLINE]

10:  Cooper AF, Yu KP, Brueckner M, Brailey LL, Johnson L, McGrath JM, Bale AE. 
 Cardiac and CNS defects in a mouse with targeted disruption of suppressor of
fused.
Development. 2005 Oct;132(19):4407-17. 
PMID: 16155214 [PubMed - indexed for MEDLINE]

11:  Klein RD, Salih S, Bessoni J, Bale AE. 
 Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic
laboratory.
Genet Med. 2005 Feb;7(2):131-8. 
PMID: 15714081 [PubMed - indexed for MEDLINE]

12:  Busygina V, Suphapeetiporn K, Marek LR, Stowers RS, Xu T, Bale AE. 
 Hypermutability in a Drosophila model for multiple endocrine neoplasia type 1.
Hum Mol Genet. 2004 Oct 15;13(20):2399-408. Epub 2004 Aug 27. 
PMID: 15333582 [PubMed - indexed for MEDLINE]

13:  Choi DH, Lee MH, Bale AE, Carter D, Haffty BG. 
 Incidence of BRCA1 and BRCA2 mutations in young Korean breast cancer patients.
J Clin Oncol. 2004 May 1;22(9):1638-45. 
PMID: 15117986 [PubMed - indexed for MEDLINE]

14:  Barreto DC, Bale AE, De Marco L, Gomez RS. 
 Immunolocalization of PTCH protein in odontogenic cysts and tumors.
J Dent Res. 2002 Nov;81(11):757-60. 
PMID: 12407090 [PubMed - indexed for MEDLINE]

15:  Suphapeetiporn K, Greally JM, Walpita D, Ashley T, Bale AE. 
 MEN1 tumor-suppressor protein localizes to telomeres during meiosis.
Genes Chromosomes Cancer. 2002 Sep;35(1):81-5. 
PMID: 12203793 [PubMed - indexed for MEDLINE]

16:  Bale AE. 
 Hedgehog signaling and human disease.
Annu Rev Genomics Hum Genet. 2002;3:47-65. Epub 2002 Apr 15. Review. 
PMID: 12142354 [PubMed - indexed for MEDLINE]

17:  Haffty BG, Harrold E, Khan AJ, Pathare P, Smith TE, Turner BC, Glazer PM,
Ward B, Carter D, Matloff E, Bale AE, Alvarez-Franco M. 
 Outcome of conservatively managed early-onset breast cancer by BRCA1/2 status.
Lancet. 2002 Apr 27;359(9316):1471-7. 
PMID: 11988246 [PubMed - indexed for MEDLINE]

18:  Llort G, Munoz CY, Tuser MP, Guillermo IB, Lluch JR, Bale AE, Franco MA. 
 Low frequency of recurrent BRCA1 and BRCA2 mutations in Spain.
Hum Mutat. 2002 Mar;19(3):307. 
PMID: 11857748 [PubMed - indexed for MEDLINE]

19:  Raymond K, Bale AE, Barnes CA, Rinaldo P. 
 Medium-chain acyl-CoA dehydrogenase deficiency: sudden and unexpected death of
a 45 year old woman.
Genet Med. 1999 Sep-Oct;1(6):293-4. No abstract available. 
PMID: 11258631 [PubMed - indexed for MEDLINE]

20:  Bale AE, Yu  KP. 
 The hedgehog pathway and basal cell carcinomas.
Hum Mol Genet. 2001 Apr;10(7):757-62. Review. 
PMID: 11257109 [PubMed - indexed for MEDLINE]

21:  Taylor TJ, Donlon SS, Bale AE, Smallridge RC, Francis TB, Christensen RS,
Burma KD. 
 Treatment of a thyrotropinoma with octreotide-LAR in a patient with multiple
endocrine neoplasia-1.
Thyroid. 2000 Nov;10(11):1001-7. 
PMID: 11128714 [PubMed - indexed for MEDLINE]

22:  Bale AE. 
 Sheep, lilies and human genetics.
Nature. 2000 Aug 31;406(6799):944-5. No abstract available. 
PMID: 10984033 [PubMed - indexed for MEDLINE]

23:  Barreto DC, Gomez RS, Bale AE, Boson WL, De Marco L. 
 PTCH gene mutations in odontogenic keratocysts.
J Dent Res. 2000 Jun;79(6):1418-22. 
PMID: 10890722 [PubMed - indexed for MEDLINE]

24:  Dong J, Gailani MR, Pomeroy SL, Reardon D, Bale AE. 
 Identification of PATCHED mutations in medulloblastomas by direct sequencing.
Hum Mutat. 2000 Jul;16(1):89-90. 
PMID: 10874314 [PubMed - indexed for MEDLINE]

25:  Gailani MR, Bale AE. 
 Acquired and inherited basal cell carcinomas and the patched gene.
Adv Dermatol. 1999;14:261-83; discussion 284. Review. No abstract available. 
PMID: 10643501 [PubMed - indexed for MEDLINE]

26:  Bale AE. 
 Prenatal diagnosis of ornithine transcarbamylase deficiency.
Prenat Diagn. 1999 Nov;19(11):1052-4. Review. No abstract available. 
PMID: 10589058 [PubMed - indexed for MEDLINE]

27:  Heptulla RA, Schwartz RP, Bale AE, Flynn S, Genel M. 
 Familial medullary thyroid carcinoma: presymptomatic diagnosis and management
in children.
J Pediatr. 1999 Sep;135(3):327-31. 
PMID: 10484798 [PubMed - indexed for MEDLINE]

28:  Petroianu A, Boson WL, Bale AE, Friedman E, De Marco L. 
 Mutational analyses of candidate genes in human squamous cell carcinomas.
Laryngoscope. 1999 Apr;109(4):661-3. 
PMID: 10201760 [PubMed - indexed for MEDLINE]

29:  Topaloglu AK, Sansaricq C, Fox JE, Bale AE, Tuchman M, Desnick RJ. 
 Prenatal molecular diagnosis of severe ornithine carbamoyltransferase
deficiency due to a novel mutation, E181G.
J Inherit Metab Dis. 1999 Feb;22(1):82-3. No abstract available. 
PMID: 10070622 [PubMed - indexed for MEDLINE]

30:  Wicking C, Bale AE. 
 Molecular basis of the nevoid basal cell carcinoma syndrome.
Curr Opin Pediatr. 1997 Dec;9(6):630-5. Review. 
PMID: 9425597 [PubMed - indexed for MEDLINE]

31:  Gailani MR, Bale AE. 
 Developmental genes and cancer: role of patched in basal cell carcinoma of the
skin.
J Natl Cancer Inst. 1997 Aug 6;89(15):1103-9. Review. 
PMID: 9262247 [PubMed - indexed for MEDLINE]

32:  Walter AW, Pivnick EK, Bale AE, Kun LE. 
 Complications of the nevoid basal cell carcinoma syndrome: a case report.
J Pediatr Hematol Oncol. 1997 May-Jun;19(3):258-62. 
PMID: 9201152 [PubMed - indexed for MEDLINE]

33:  Kimonis VE, Goldstein AM, Pastakia B, Yang ML, Kase R, DiGiovanna JJ, Bale
AE, Bale SJ. 
 Clinical manifestations in 105 persons with nevoid basal cell carcinoma
syndrome.
Am J Med Genet. 1997 Mar 31;69(3):299-308. Review. 
PMID: 9096761 [PubMed - indexed for MEDLINE]

34:  Chidambaram A, Gailani M, Gerrard B, Stewart C, Goldstein A, Chumakov I,
Bale AE, Dean M. 
 Characterization of a YAC contig containing the NBCCS locus and a novel
Kruppel-type zinc finger sequence on chromosome segment 9q22.3.
Genes Chromosomes Cancer. 1997 Mar;18(3):212-8. 
PMID: 9071574 [PubMed - indexed for MEDLINE]

35:  Levanat S, Chidambaram A, Wicking C, Bray-Ward P, Pressman C, Toftgard R,
Gailani MR, Myers JC, Wainwright B, Dean M, Bale AE. 
 Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement
of a novel zinc finger gene within the NBCCS and ESS1 region.
Cytogenet Cell Genet. 1997;76(3-4):208-13. 
PMID: 9186526 [PubMed - indexed for MEDLINE]

36:  Bale AE. 
 The nevoid basal cell carcinoma syndrome: genetics and mechanism of
carcinogenesis.
Cancer Invest. 1997;15(2):180-6. Review. 
PMID: 9095215 [PubMed - indexed for MEDLINE]

37:  Bale AE. 
 Variable expressivity of patched mutations in flies and humans.
Am J Hum Genet. 1997 Jan;60(1):10-2. No abstract available. 
PMID: 8981940 [PubMed - indexed for MEDLINE]

38:  Chidambaram A, Goldstein AM, Gailani MR, Gerrard B, Bale SJ, DiGiovanna JJ,
Bale AE, Dean M. 
 Mutations in the human homologue of the Drosophila patched gene in Caucasian
and African-American nevoid basal cell carcinoma syndrome patients.
Cancer Res. 1996 Oct 15;56(20):4599-601. 
PMID: 8840969 [PubMed - indexed for MEDLINE]

39:  Gailani MR, Stahle-Backdahl M, Leffell DJ, Glynn M, Zaphiropoulos PG,
Pressman C, Unden AB, Dean M, Brash DE, Bale AE, Toftgard R. 
 The role of the human homologue of Drosophila patched in sporadic basal cell
carcinomas.
Nat Genet. 1996 Sep;14(1):78-81. 
PMID: 8782823 [PubMed - indexed for MEDLINE]

40:  Shimkets R, Gailani MR, Siu VM, Yang-Feng T, Pressman CL, Levanat S,
Goldstein A, Dean M, Bale AE. 
 Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients.
Am J Hum Genet. 1996 Aug;59(2):417-22. 
PMID: 8755929 [PubMed - indexed for MEDLINE]

41:  Hahn H, Wicking C, Zaphiropoulous PG, Gailani MR, Shanley S, Chidambaram A,
Vorechovsky I, Holmberg E, Unden AB, Gillies S, Negus K, Smyth I, Pressman C,
Leffell DJ, Gerrard B, Goldstein AM, Dean M, Toftgard R, Chenevix-Trench G,
Wainwright B, Bale AE. 
 Mutations of the human homolog of Drosophila patched in the nevoid basal cell
carcinoma syndrome.
Cell. 1996 Jun 14;85(6):841-51. 
PMID: 8681379 [PubMed - indexed for MEDLINE]

42:  Petrikovsky BM, Bialer MG, McLaughlin JA, Bale AE. 
 Sonographic and DNA-based prenatal detection of Gorlin syndrome.
J Ultrasound Med. 1996 Jun;15(6):493-5. No abstract available. 
PMID: 8738998 [PubMed - indexed for MEDLINE]

43:  Hahn H, Christiansen J, Wicking C, Zaphiropoulos PG, Chidambaram A, Gerrard
B, Vorechovsky I, Bale AE, Toftgard R, Dean M, Wainwright B. 
 A mammalian patched homolog is expressed in target tissues of sonic hedgehog
and maps to a region associated with developmental abnormalities.
J Biol Chem. 1996 May 24;271(21):12125-8. 
PMID: 8647801 [PubMed - indexed for MEDLINE]

44:  Gailani MR, Leffell DJ, Ziegler A, Gross EG, Brash DE, Bale AE. 
 Relationship between sunlight exposure and a key genetic alteration in basal
cell carcinoma.
J Natl Cancer Inst. 1996 Mar 20;88(6):349-54. 
PMID: 8609643 [PubMed - indexed for MEDLINE]

45:  Levanat S, Gorlin RJ, Fallet S, Johnson DR, Fantasia JE, Bale AE. 
 A two-hit model for developmental defects in Gorlin syndrome.
Nat Genet. 1996 Jan;12(1):85-7. No abstract available. 
PMID: 8528259 [PubMed - indexed for MEDLINE]

46:  Johnson DR, Levanat S, Bale AE. 
 Direct molecular analysis of archival tumor tissue for loss of heterozygosity.
Biotechniques. 1995 Aug;19(2):190-2. No abstract available. 
PMID: 8527133 [PubMed - indexed for MEDLINE]

47:  Bale AE, Gailani MR, Leffell DJ. 
 The Gorlin syndrome gene: a tumor suppressor active in basal cell
carcinogenesis and embryonic development.
Proc Assoc Am Physicians. 1995 Jul;107(2):253-7. Review. No abstract available. 
PMID: 8624861 [PubMed - indexed for MEDLINE]

48:  Cox DW, Billingsley GD, Bale AE, Donis-Keller H, Edwards JH, Litt M,
Mcbride W, Persichetti F, Spurr NK, Weber JL, et al. 
 CEPH consortium map of chromosome 14.
Cytogenet Cell Genet. 1995;69(3-4):175-8. 
PMID: 7698005 [PubMed - indexed for MEDLINE]

49:  Bale AE, Gailani MR, Leffell DJ. 
 Nevoid basal cell carcinoma syndrome.
J Invest Dermatol. 1994 Nov;103(5 Suppl):126S-130S. Review. 
PMID: 7963674 [PubMed - indexed for MEDLINE]

50:  Friedman E, Bale AE, Carson E, Boson WL, Nordenskjold M, Ritzen M, Ferreira
PC, Jammal A, De Marco L. 
 Nephrogenic diabetes insipidus: an X chromosome-linked dominant inheritance
pattern with a vasopressin type 2 receptor gene that is structurally normal.
Proc Natl Acad Sci U S A. 1994 Aug 30;91(18):8457-61. 
PMID: 8078903 [PubMed - indexed for MEDLINE]

51:  Bialer MG, Gailani MR, McLaughlin JA, Petrikovsky B, Bale AE. 
 Prenatal diagnosis of Gorlin syndrome.
Lancet. 1994 Aug 13;344(8920):477. No abstract available. 
PMID: 7914587 [PubMed - indexed for MEDLINE]

52:  Compton JG, Goldstein AM, Turner M, Bale AE, Kearns KS, McBride OW, Bale
SJ. 
 Fine mapping of the locus for nevoid basal cell carcinoma syndrome on
chromosome 9q.
J Invest Dermatol. 1994 Aug;103(2):178-81. 
PMID: 8040607 [PubMed - indexed for MEDLINE]

53:  Petty EM, Green JS, Marx SJ, Taggart RT, Farid N, Bale AE. 
 Mapping the gene for hereditary hyperparathyroidism and prolactinoma
(MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from
Newfoundland.
Am J Hum Genet. 1994 Jun;54(6):1060-6. 
PMID: 7911003 [PubMed - indexed for MEDLINE]

54:  Goldstein AM, Stewart C, Bale AE, Bale SJ, Dean M. 
 Localization of the gene for the nevoid basal cell carcinoma syndrome.
Am J Hum Genet. 1994 May;54(5):765-73. 
PMID: 7909984 [PubMed - indexed for MEDLINE]

55:  Goldstein AM, Pastakia B, DiGiovanna JJ, Poliak S, Santucci S, Kase R, Bale
AE, Bale SJ. 
 Clinical findings in two African-American families with the nevoid basal cell
carcinoma syndrome (NBCC).
Am J Med Genet. 1994 Apr 15;50(3):272-81. Review. 
PMID: 8042672 [PubMed - indexed for MEDLINE]

56:  Bale AE. 
 Molecular mechanisms of neoplasia in multiple endocrine neoplasia type
1-related and sporadic tumors of the pancreatic islet cells.
Endocrinol Metab Clin North Am. 1994 Mar;23(1):109-15. Review. 
PMID: 7913019 [PubMed - indexed for MEDLINE]

57:  Petty EM, Gibson LH, Fountain JW, Bolognia JL, Yang-Feng TL, Housman DE,
Bale AE. 
 Molecular definition of a chromosome 9p21 germ-line deletion in a woman with
multiple melanomas and a plexiform neurofibroma: implications for 9p
tumor-suppressor gene(s).
Am J Hum Genet. 1993 Jul;53(1):96-104. 
PMID: 8317504 [PubMed - indexed for MEDLINE]

58:  Ziegler A, Leffell DJ, Kunala S, Sharma HW, Gailani M, Simon JA, Halperin
AJ, Baden HP, Shapiro PE, Bale AE, et al. 
 Mutation hotspots due to sunlight in the p53 gene of nonmelanoma skin cancers.
Proc Natl Acad Sci U S A. 1993 May 1;90(9):4216-20. 
PMID: 8483937 [PubMed - indexed for MEDLINE]

59:  Petty EM, Arnold A, Marx SJ, Bale AE. 
 A pulsed-field gel electrophoresis (PFGE) map of twelve loci on chromosome
11q11-q13.
Genomics. 1993 Feb;15(2):423-5. 
PMID: 8449512 [PubMed - indexed for MEDLINE]

60:  Falchetti A, Bale AE, Amorosi A, Bordi C, Cicchi P, Bandini S, Marx SJ,
Brandi ML. 
 Progression of uremic hyperparathyroidism involves allelic loss on chromosome
11.
J Clin Endocrinol Metab. 1993 Jan;76(1):139-44. 
PMID: 8421078 [PubMed - indexed for MEDLINE]

61:  Petty EM, Bolognia JL, Bale AE, Yang-Feng T. 
 Cutaneous malignant melanoma and atypical moles associated with a
constitutional rearrangement of chromosomes 5 and 9.
Am J Med Genet. 1993 Jan 1;45(1):77-80. 
PMID: 8418665 [PubMed - indexed for MEDLINE]

62:  Kwiatkowski DJ, Armour J, Bale AE, Fountain JW, Goudie D, Haines JL,
Knowles MA, Pilz A, Slaugenhaupt S, Povey S. 
 Report and abstracts of the Second International Workshop on Human Chromosome 9
Mapping 1993.
Cytogenet Cell Genet. 1993;64(2):93-121. No abstract available. 
PMID: 8334899 [PubMed - indexed for MEDLINE]

63:  Friedman E, De Marco L, Gejman PV, Norton JA, Bale AE, Aurbach GD, Spiegel
AM, Marx SJ. 
 Allelic loss from chromosome 11 in parathyroid tumors.
Cancer Res. 1992 Dec 15;52(24):6804-9. 
PMID: 1360870 [PubMed - indexed for MEDLINE]

64:  Petty EM, Gold E, Bale AE. 
 DNA diagnosis with mutation-specific artificial methylation sites: application
to rapid screening of delta F508.
Clin Chem. 1992 Dec;38(12):2422-5. 
PMID: 1458578 [PubMed - indexed for MEDLINE]

65:  Cannon-Albright LA, Goldgar DE, Meyer LJ, Lewis CM, Anderson DE, Fountain
JW, Hegi ME, Wiseman RW, Petty EM, Bale AE, et al. 
 Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22.
Science. 1992 Nov 13;258(5085):1148-52. 
PMID: 1439824 [PubMed - indexed for MEDLINE]

66:  Mitchell A, Bale AE, Lee BJ, Hatfield D, Harley H, Rundle SA, Fan YS,
Fukushima Y, Shows TB, McBride OW. 
 Regional localization of the selenocysteine tRNA gene (TRSP) on human
chromosome 19.
Cytogenet Cell Genet. 1992;61(2):117-20. 
PMID: 1395717 [PubMed - indexed for MEDLINE]

67:  Mitchell A, Bale AE, Wang-Ge M, Yi HF, White R, Pirtle RM, McBride OW. 
 Localization of a DNA segment encompassing four tRNA genes to human chromosome
14q11 and its use as an anchor locus for linkage analysis.
Genomics. 1991 Dec;11(4):1063-70. 
PMID: 1686015 [PubMed - indexed for MEDLINE]

68:  Bowcock AM, Farrer LA, Hebert JM, Bale AE, Cavalli-Sforza L. 
 A contiguous linkage map of chromosome 13q with 39 distinct loci separated on
average by 5.1 centimorgans.
Genomics. 1991 Nov;11(3):517-29. 
PMID: 1685473 [PubMed - indexed for MEDLINE]

69:  Rosenberg CL, Wong E, Petty EM, Bale AE, Tsujimoto Y, Harris NL, Arnold A. 
 PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic
lymphoma.
Proc Natl Acad Sci U S A. 1991 Nov 1;88(21):9638-42. 
PMID: 1682919 [PubMed - indexed for MEDLINE]

70:  Bale SJ, Amos CI, Parry DM, Bale AE. 
 Relationship between head circumference and height in normal adults and in the
nevoid basal cell carcinoma syndrome and neurofibromatosis type I.
Am J Med Genet. 1991 Aug 1;40(2):206-10. 
PMID: 1910262 [PubMed - indexed for MEDLINE]

71:  Bale AE, Mitchell AL, Gonzalez FJ, McBride OW. 
 Localization of CYP2F1 by multipoint linkage analysis and pulsed-field gel
electrophoresis.
Genomics. 1991 May;10(1):284-6. 
PMID: 2045106 [PubMed - indexed for MEDLINE]

72:  Petersen DD, McKinney CE, Ikeya K, Smith HH, Bale AE, McBride OW, Nebert
DW. 
 Human CYP1A1 gene: cosegregation of the enzyme inducibility phenotype and an
RFLP.
Am J Hum Genet. 1991 Apr;48(4):720-5. 
PMID: 1707592 [PubMed - indexed for MEDLINE]

73:  Fein HG, Burman KD, Djuh YY, Usala SJ, Bale AE, Weintraub BD, Smallridge
RC. 
 Tight linkage of the human c-erbA beta gene with the syndrome of generalized
thyroid hormone resistance is present in multiple kindreds.
J Endocrinol Invest. 1991 Mar;14(3):219-23. 
PMID: 1677017 [PubMed - indexed for MEDLINE]

74:  Bale AE, Norton JA, Wong EL, Fryburg JS, Maton PN, Oldfield EH, Streeten E,
Aurbach GD, Brandi ML, Friedman E, et al. 
 Allelic loss on chromosome 11 in hereditary and sporadic tumors related to
familial multiple endocrine neoplasia type 1.
Cancer Res. 1991 Feb 15;51(4):1154-7. 
PMID: 1671755 [PubMed - indexed for MEDLINE]

75:  Petty EM, Carstens R, Bale AE. 
 Ornithine transcarbamylase polymorphism detected by PCR introduction of DraI
site.
Nucleic Acids Res. 1991 Feb 11;19(3):690. No abstract available. 
PMID: 2011544 [PubMed - indexed for MEDLINE]

76:  Usala SJ, Menke JB, Watson TL, Berard WE, Bradley C, Bale AE, Lash RW,
Weintraub BD. 
 A new point mutation in the 3,5,3'-triiodothyronine-binding domain of the
c-erbA beta thyroid hormone receptor is tightly linked to generalized thyroid
hormone resistance.
J Clin Endocrinol Metab. 1991 Jan;72(1):32-8. 
PMID: 1846005 [PubMed - indexed for MEDLINE]

77:  Solomon SD, Geisterfer-Lowrance AA, Vosberg HP, Hiller G, Jarcho JA, Morton
CC, McBride WO, Mitchell AL, Bale AE, McKenna WJ, et al. 
 A locus for familial hypertrophic cardiomyopathy is closely linked to the
cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at
q11-q12.
Am J Hum Genet. 1990 Sep;47(3):389-94. 
PMID: 1975475 [PubMed - indexed for MEDLINE]

78:  Wong EL, Kandpal G, Bale AE. 
 Two RFLPs at the glutathione S-transferase 3 gene.
Nucleic Acids Res. 1990 Aug 25;18(16):4964. No abstract available. 
PMID: 1975681 [PubMed - indexed for MEDLINE]

79:  Friedman E, Bale AE, Marx SJ, Norton JA, Arnold A, Tu T, Aurbach GD,
Spiegel AM. 
 Genetic abnormalities in sporadic parathyroid adenomas.
J Clin Endocrinol Metab. 1990 Aug;71(2):293-7. 
PMID: 2199477 [PubMed - indexed for MEDLINE]

80:  Nakayama Y, Wondisford FE, Lash RW, Bale AE, Weintraub BD, Cutler GB Jr,
Radovick S. 
 Analysis of gonadotropin-releasing hormone gene structure in families with
familial central precocious puberty and idiopathic hypogonadotropic
hypogonadism.
J Clin Endocrinol Metab. 1990 May;70(5):1233-8. 
PMID: 2186053 [PubMed - indexed for MEDLINE]

81:  Usala SJ, Tennyson GE, Bale AE, Lash RW, Gesundheit N, Wondisford FE,
Accili D, Hauser P, Weintraub BD. 
 A base mutation of the C-erbA beta thyroid hormone receptor in a kindred with
generalized thyroid hormone resistance. Molecular heterogeneity in two other
kindreds.
J Clin Invest. 1990 Jan;85(1):93-100. 
PMID: 2153155 [PubMed - indexed for MEDLINE]

82:  Bale AE, Bale SJ, Murli H, Ivett J, Mulvihill JJ, Parry DM. 
 Sister chromatid exchange and chromosome fragility in the nevoid basal cell
carcinoma syndrome.
Cancer Genet Cytogenet. 1989 Oct 15;42(2):273-9. 
PMID: 2507127 [PubMed - indexed for MEDLINE]

83:  Friedman E, Sakaguchi K, Bale AE, Falchetti A, Streeten E, Zimering MB,
Weinstein LS, McBride WO, Nakamura Y, Brandi ML, et al. 
 Clonality of parathyroid tumors in familial multiple endocrine neoplasia type
1.
N Engl J Med. 1989 Jul 27;321(4):213-8. Erratum in: N Engl J Med 1989 Oct
12;321(15):1057. 
PMID: 2568586 [PubMed - indexed for MEDLINE]

84:  Mitchell AL, Bale AE, Mak T, McBride OW. 
 Six RFLPs for human T cell receptor alpha (TCRA) on chromosome 14.
Nucleic Acids Res. 1989 Apr 11;17(7):2876. No abstract available. 
PMID: 2566151 [PubMed - indexed for MEDLINE]

85:  Bale SJ, Bale AE, Stewart K, Dachowski L, McBride OW, Glaser T, Green JE
3rd, Mulvihill JJ, Brandi ML, Sakaguchi K, et al. 
 Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other
markers on chromosome 11.
Genomics. 1989 Apr;4(3):320-2. Erratum in: Genomics 1989 Jul;5(1):166. 
PMID: 2565877 [PubMed - indexed for MEDLINE]

86:  Usala SJ, Bale AE, Gesundheit N, Weinberger C, Lash RW, Wondisford FE,
McBride OW, Weintraub BD. 
 Tight linkage between the syndrome of generalized thyroid hormone resistance
and the human c-erbA beta gene.
Mol Endocrinol. 1988 Dec;2(12):1217-20. 
PMID: 2905763 [PubMed - indexed for MEDLINE]

87:  Bale AE, Usala S, Weinberger C, Weintraub BD, McBride OW. 
 A cDNA probe (PheA12) from the hc-(ERBA) gene on chromosome 3 detects a high
frequency RFLP.
Nucleic Acids Res. 1988 Aug 11;16(15):7756. No abstract available. 
PMID: 2901070 [PubMed - indexed for MEDLINE]

88:  Bale AE, Weinberger C, McBride OW. 
 A retinoic acid receptor cDNA probe (RAR2) identifies a moderately frequent
RFLP on chromosome 17.
Nucleic Acids Res. 1988 Aug 11;16(15):7755. No abstract available. 
PMID: 2901069 [PubMed - indexed for MEDLINE]

89:  Bale AE, Bale SJ, Schlesinger SL, McFarland HF. 
 Linkage analysis in spinopontine atrophy: correlation of HLA linkage with
phenotypic findings in hereditary ataxia.
Am J Med Genet. 1987 Jul;27(3):595-602. 
PMID: 3477098 [PubMed - indexed for MEDLINE]

90:  Bale AE. 
 Internal malignancy in genetic hemochromatosis.
J Natl Cancer Inst. 1986 Jun;76(6):1260-1. No abstract available. 
PMID: 3012180 [PubMed - indexed for MEDLINE]

91:  Bale SJ, Harris EL, Bale AE. 
 Linkage relationships among four 11p markers in the Utah dataset.
Genet Epidemiol Suppl. 1986;1:117-21. No abstract available. 
PMID: 3471653 [PubMed - indexed for MEDLINE]

92:  Bale AE, Ludwig IH, Effron LA, Zakov ZN. 
 Linkage between the genes for Wolfram syndrome and brachydactyly E.
Am J Med Genet. 1985 Apr;20(4):733-4. No abstract available. 
PMID: 3993691 [PubMed - indexed for MEDLINE]

93:  Bale AE, Drum MA, Parry DM, Mulvihill JJ. 
 Familial Sotos syndrome (cerebral gigantism): craniofacial and psychological
characteristics.
Am J Med Genet. 1985 Apr;20(4):613-24. 
PMID: 2581446 [PubMed - indexed for MEDLINE]