Feingold J - Search Results

1

Parental consanguinity as a cause of increased incidence of birth defects in a study of 131,760 consecutive births.

Stoll C, Alembik Y, Dott B, Feingold J. Stoll C, et al. Among authors: feingold j. Am J Med Genet. 1994 Jan 1;49(1):114-7. doi: 10.1002/ajmg.1320490123. Am J Med Genet. 1994. PMID: 7864918

2

Reply to Newton Freire-Maia on inbreeding among medical geneticists II.

Stoll C, Alembik Y, Dott B, Feingold J. Stoll C, et al. Among authors: feingold j. Am J Med Genet. 1995 Jul 3;57(3):507. doi: 10.1002/ajmg.1320570334. Am J Med Genet. 1995. PMID: 7677164 No abstract available.

3

Transforming growth factor-alpha: characterization of the BamHI, RsaI, and TaqI polymorphic regions.

Qian JF, Feingold J, Stoll C, May E. Qian JF, et al. Among authors: feingold j. Am J Hum Genet. 1993 Jul;53(1):168-75. Am J Hum Genet. 1993. PMID: 8100397 Free PMC article.

4

Genetic variation in transforming growth factor alpha: possible association of BamHI polymorphism with bilateral sporadic cleft lip and palate.

Stoll C, Qian JF, Feingold J, Sauvage P, May E. Stoll C, et al. Among authors: feingold j. Hum Genet. 1993 Aug;92(1):81-2. doi: 10.1007/BF00216150. Hum Genet. 1993. PMID: 8103504

5

No evidence for genomic imprinting in liver-born Down syndrome patients.

Stoll C, Alembik Y, Dott B, Feingold J. Stoll C, et al. Among authors: feingold j. Acta Genet Med Gemellol (Roma). 1996;45(1-2):265-71. doi: 10.1017/s0001566000001434. Acta Genet Med Gemellol (Roma). 1996. PMID: 8872044

6

Do parents and grandparents of patients with achondroplasia have a higher cancer risk?

Stoll C, Feingold J. Stoll C, et al. Among authors: feingold j. Am J Med Genet A. 2004 Oct 1;130A(2):165-8. doi: 10.1002/ajmg.a.30273. Am J Med Genet A. 2004. PMID: 15372518

7

No evidence for genomic imprinting in liveborn Down syndrome patients.

Stoll C, Alembik Y, Dott B, Feingold J. Stoll C, et al. Among authors: feingold j. Ann Genet. 1995;38(1):13-8. Ann Genet. 1995. PMID: 7625754

8

Clinical homogeneity and genetic heterogeneity in Weill-Marchesani syndrome.

Faivre L, Dollfus H, Lyonnet S, Alembik Y, Mégarbané A, Samples J, Gorlin RJ, Alswaid A, Feingold J, Le Merrer M, Munnich A, Cormier-Daire V. Faivre L, et al. Among authors: feingold j. Am J Med Genet A. 2003 Dec 1;123A(2):204-7. doi: 10.1002/ajmg.a.20289. Am J Med Genet A. 2003. PMID: 14598350 Review.

9

Genetic variation in transforming growth factor alpha: possible association of BamHI polymorphism with bilateral sporadic cleft lip and palate.

Stoll C, Qian JF, Feingold J, Sauvage P, May E. Stoll C, et al. Among authors: feingold j. Am J Hum Genet. 1992 Apr;50(4):870-1. Am J Hum Genet. 1992. PMID: 1347971 Free PMC article. No abstract available.

10

A novel BamHI polymorphism for the human transforming growth factor alpha gene (TGF-alpha).

Qian JF, May E, Feingold J, Stoll C. Qian JF, et al. Among authors: feingold j. Nucleic Acids Res. 1991 Dec 11;19(23):6665. doi: 10.1093/nar/19.23.6665. Nucleic Acids Res. 1991. PMID: 1684429 Free PMC article.

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