Hecht JT - Search Results

1

Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11.

Wuyts W, Ramlakhan S, Van Hul W, Hecht JT, van den Ouweland AM, Raskind WH, Hofstede FC, Reyniers E, Wells DE, de Vries B, et al. Wuyts W, et al. Among authors: hecht jt. Am J Hum Genet. 1995 Aug;57(2):382-7. Am J Hum Genet. 1995. PMID: 7668264 Free PMC article.

2

Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.

Bartsch O, Wuyts W, Van Hul W, Hecht JT, Meinecke P, Hogue D, Werner W, Zabel B, Hinkel GK, Powell CM, Shaffer LG, Willems PJ. Bartsch O, et al. Among authors: hecht jt. Am J Hum Genet. 1996 Apr;58(4):734-42. Am J Hum Genet. 1996. PMID: 8644736 Free PMC article.

3

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.

4

Hereditary multiple exostoses: confirmation of linkage to chromosomes 8 and 11.

Blanton SH, Hogue D, Wagner M, Wells D, Young ID, Hecht JT. Blanton SH, et al. Among authors: hecht jt. Am J Med Genet. 1996 Mar 15;62(2):150-9. doi: 10.1002/(SICI)1096-8628(19960315)62:2<150::AID-AJMG7>3.0.CO;2-#. Am J Med Genet. 1996. PMID: 8882395

5

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.

6

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

7

Evidence, from family studies, for linkage disequilibrium between TGFA and a gene for nonsyndromic cleft lip with or without cleft palate.

Feng H, Sassani R, Bartlett SP, Lee A, Hecht JT, Malcolm S, Winter RM, Vintiner GM, Buetow KH, Gasser DL. Feng H, et al. Among authors: hecht jt. Am J Hum Genet. 1994 Nov;55(5):932-6. Am J Hum Genet. 1994. PMID: 7977355 Free PMC article.

8

Natural history study of hereditary multiple exostoses.

Wicklund CL, Pauli RM, Johnston D, Hecht JT. Wicklund CL, et al. Among authors: hecht jt. Am J Med Genet. 1995 Jan 2;55(1):43-6. doi: 10.1002/ajmg.1320550113. Am J Med Genet. 1995. PMID: 7702095

9

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.

10

Construction of a natural panel of 11p11.2 deletions and further delineation of the critical region involved in Potocki-Shaffer syndrome.

Wakui K, Gregato G, Ballif BC, Glotzbach CD, Bailey KA, Kuo PL, Sue WC, Sheffield LJ, Irons M, Gomez EG, Hecht JT, Potocki L, Shaffer LG. Wakui K, et al. Among authors: hecht jt. Eur J Hum Genet. 2005 May;13(5):528-40. doi: 10.1038/sj.ejhg.5201366. Eur J Hum Genet. 2005. PMID: 15852040

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