Hecht JT - Search Results

1

Studies of TBX4 and chromosome 17q23.1q23.2: an uncommon cause of nonsyndromic clubfoot.

Lu W, Bacino CA, Richards BS, Alvarez C, VanderMeer JE, Vella M, Ahituv N, Sikka N, Dietz FR, Blanton SH, Hecht JT. Lu W, et al. Among authors: hecht jt. Am J Med Genet A. 2012 Jul;158A(7):1620-7. doi: 10.1002/ajmg.a.35418. Epub 2012 Jun 7. Am J Med Genet A. 2012. PMID: 22678995 Free PMC article.

2

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

3

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.

4

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.

5

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.

6

Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families.

Stein J, Mulliken JB, Stal S, Gasser DL, Malcolm S, Winter R, Blanton SH, Amos C, Seemanova E, Hecht JT. Stein J, et al. Among authors: hecht jt. Am J Hum Genet. 1995 Aug;57(2):257-72. Am J Hum Genet. 1995. PMID: 7668251 Free PMC article.

7

Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia.

Hecht JT, Nelson LD, Crowder E, Wang Y, Elder FF, Harrison WR, Francomano CA, Prange CK, Lennon GG, Deere M, et al. Hecht JT, et al. Nat Genet. 1995 Jul;10(3):325-9. doi: 10.1038/ng0795-325. Nat Genet. 1995. PMID: 7670471

8

Confirmatory linkage of hypochondroplasia to chromosome arm 4p.

Hecht JT, Herrera CA, Greenhaw GA, Francomano CA, Bellus GA, Blanton SH. Hecht JT, et al. Am J Med Genet. 1995 Jul 3;57(3):505-6. doi: 10.1002/ajmg.1320570333. Am J Med Genet. 1995. PMID: 7677163 No abstract available.

9

Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8.

Hecht JT, Hogue D, Strong LC, Hansen MF, Blanton SH, Wagner M. Hecht JT, et al. Am J Hum Genet. 1995 May;56(5):1125-31. Am J Hum Genet. 1995. PMID: 7726168 Free PMC article.

10

Genetic heterogeneity in multiple epiphyseal dysplasia.

Deere M, Blanton SH, Scott CI, Langer LO, Pauli RM, Hecht JT. Deere M, et al. Among authors: hecht jt. Am J Hum Genet. 1995 Mar;56(3):698-704. Am J Hum Genet. 1995. PMID: 7887425 Free PMC article.

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