Hecht JT - Search Results

1

Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies.

Hecht JT, Hogue D, Wang Y, Blanton SH, Wagner M, Strong LC, Raskind W, Hansen MF, Wells D. Hecht JT, et al. Am J Hum Genet. 1997 Jan;60(1):80-6. Am J Hum Genet. 1997. PMID: 8981950 Free PMC article.

2

Polymorphic dinucleotide repeat in a cartilage matrix protein (CRTM) gene.

Wang Y, Sadler L, Hecht JT. Wang Y, et al. Among authors: hecht jt. Hum Mol Genet. 1992 Dec;1(9):780. doi: 10.1093/hmg/1.9.780-a. Hum Mol Genet. 1992. PMID: 1302624 No abstract available.

3

Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes.

Greenhaw GA, Hebert A, Duke-Woodside ME, Butler IJ, Hecht JT, Cleaver JE, Thomas GH, Horton WA. Greenhaw GA, et al. Among authors: hecht jt. Am J Hum Genet. 1992 Apr;50(4):677-89. Am J Hum Genet. 1992. PMID: 1372469 Free PMC article.

4

Exclusion of human proteoglycan link protein (CRTL1) and type II collagen (COL2A1) genes in pseudoachondroplasia.

Hecht JT, Blanton SH, Wang Y, Daiger SP, Horton WA, Rhodes C, Yamada Y, Francomano CA. Hecht JT, et al. Am J Med Genet. 1992 Nov 1;44(4):420-4. doi: 10.1002/ajmg.1320440406. Am J Med Genet. 1992. PMID: 1442879

5

Van der Woude syndrome and nonsyndromic cleft lip and palate.

Hecht JT, Wang Y, Blanton SH, Daiger SP. Hecht JT, et al. Am J Hum Genet. 1992 Aug;51(2):442-4. Am J Hum Genet. 1992. PMID: 1642245 Free PMC article. No abstract available.

6

Cleft lip and palate: no evidence of linkage to transforming growth factor alpha.

Hecht JT, Wang YP, Blanton SH, Michels VV, Daiger SP. Hecht JT, et al. Am J Hum Genet. 1991 Sep;49(3):682-6. Am J Hum Genet. 1991. PMID: 1679292 Free PMC article.

7

TaqI and HaeIII RFLP polymorphisms in human proteoglycan link gene (CRTL1).

Hecht JT, Wang Y, Rhodes C, Yamada Y. Hecht JT, et al. Nucleic Acids Res. 1991 Dec 11;19(23):6666. Nucleic Acids Res. 1991. PMID: 1684430 Free PMC article.

8

Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome.

Parrish JE, Wagner MJ, Hecht JT, Scott CI Jr, Wells DE. Parrish JE, et al. Among authors: hecht jt. Genomics. 1991 Sep;11(1):54-61. doi: 10.1016/0888-7543(91)90101-j. Genomics. 1991. PMID: 1684953

9

GT repeat polymorphism in the human proteoglycan link gene (CRTL1) promoter region.

Hecht JT, Wang Y, Rhodes C, Yamada Y. Hecht JT, et al. Nucleic Acids Res. 1991 Dec 11;19(23):6666. Nucleic Acids Res. 1991. PMID: 1754418 Free PMC article.

10

Complex segregation analysis of nonsyndromic cleft lip and palate.

Hecht JT, Yang P, Michels VV, Buetow KH. Hecht JT, et al. Am J Hum Genet. 1991 Sep;49(3):674-81. Am J Hum Genet. 1991. PMID: 1882845 Free PMC article.

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