Sher C - Search Results

1

Mild spondyloepiphyseal dysplasia (Namaqualand type): genetic linkage to the type II collagen gene COL2A1.

Sher C, Ramesar R, Martell R, Learmonth I, Tsipouras P, Beighton P. Sher C, et al. Am J Hum Genet. 1991 Mar;48(3):518-24. Am J Hum Genet. 1991. PMID: 1671807 Free PMC article.

2

Amegakaryocytic thrombocytopenia with duplication of part of the long arm of chromosome 3.

Hallett JM, Martell RW, Sher C, Jacobs P. Hallett JM, et al. Among authors: sher c. Br J Haematol. 1989 Feb;71(2):291-2. doi: 10.1111/j.1365-2141.1989.tb04269.x. Br J Haematol. 1989. PMID: 2923812 No abstract available.

3

High-dose busulfan and myoclonic epilepsy.

Martell RW, Sher C, Jacobs P, Monteagudo F. Martell RW, et al. Among authors: sher c. Ann Intern Med. 1987 Jan;106(1):173. doi: 10.7326/0003-4819-106-1-173_1. Ann Intern Med. 1987. PMID: 3098151 No abstract available.

4

Further delineation of cerebro-osteo-nephrosis syndrome.

Udler Y, Halpern GJ, Sher C, Davidovitz M, Shohat M. Udler Y, et al. Among authors: sher c. Am J Med Genet. 1997 Nov 12;72(4):383-5. Am J Med Genet. 1997. PMID: 9375716

5

Congenital deficiency of AFP and Down syndrome screening.

Sher C, Shohat M. Sher C, et al. Prenat Diagn. 1997 Sep;17(9):884-5. Prenat Diagn. 1997. PMID: 9316138 No abstract available.

6

Pharyngeal flap for velopharyngeal incompetence in patients with myotonic dystrophy.

Amir A, Wolf Y, Ezra Y, Shohat M, Sher C, Hauben DJ. Amir A, et al. Among authors: sher c. Ann Plast Surg. 1999 May;42(5):549-52. Ann Plast Surg. 1999. PMID: 10340866

7

Breast cancer and BRCA1 mutations.

Sher C, Sharabini-Gargir L, Shohat M. Sher C, et al. N Engl J Med. 1996 May 2;334(18):1199; author reply 1199-1200. N Engl J Med. 1996. PMID: 8602199 No abstract available.

8

Utilization of prenatal genetic testing by Israeli Moslem women: a national survey.

Sher C, Romano-Zelekha O, Green MS, Shohat T. Sher C, et al. Clin Genet. 2004 Apr;65(4):278-83. doi: 10.1111/j.1399-0004.2004.00228.x. Clin Genet. 2004. PMID: 15025719

9

A founder COL17A1 splice site mutation leading to generalized atrophic benign epidermolysis bullosa in an extended inbred Palestinian family from Israel.

Whittock NV, Sher C, Gold I, Libman V, Reish O. Whittock NV, et al. Among authors: sher c. Genet Med. 2003 Nov-Dec;5(6):435-9. doi: 10.1097/01.gim.0000096494.61125.d8. Genet Med. 2003. PMID: 14614394

10

Factors affecting performance of prenatal genetic testing by Israeli Jewish women.

Sher C, Romano-Zelekha O, Green MS, Shohat T. Sher C, et al. Am J Med Genet A. 2003 Jul 30;120A(3):418-22. doi: 10.1002/ajmg.a.20047. Am J Med Genet A. 2003. PMID: 12838566

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