Hecht JT - Search Results

1

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

2

The Nager syndrome.

Hecht JT, Immken LL, Harris LF, Malini S, Scott CI Jr. Hecht JT, et al. Am J Med Genet. 1987 Aug;27(4):965-9. doi: 10.1002/ajmg.1320270426. Am J Med Genet. 1987. PMID: 3321996

3

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.

4

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.

5

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.

6

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

7

The Schinzel syndrome in a mother and daughter.

Hecht JT, Scott CI Jr. Hecht JT, et al. Clin Genet. 1984 Jan;25(1):63-7. doi: 10.1111/j.1399-0004.1984.tb00464.x. Clin Genet. 1984. PMID: 6538465 No abstract available.

8

Limb deficiency syndrome in half-sibs.

Hecht JT, Scott CI Jr. Hecht JT, et al. Clin Genet. 1981 Dec;20(6):432-7. doi: 10.1111/j.1399-0004.1981.tb01054.x. Clin Genet. 1981. PMID: 7337959 No abstract available.

9

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.

10

A recognizable syndrome of sex-linked mental retardation, large testes, and marker X chromosome.

Hecht JT, Moore CM, Scott CI Jr. Hecht JT, et al. South Med J. 1981 Dec;74(12):1493-6. doi: 10.1097/00007611-198112000-00020. South Med J. 1981. PMID: 6947439 No abstract available.

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