Cohen T - Search Results

1

Cohen T, Zeitune M, McGillivray BC, Hall JG, Lynn AH, Aston CE, Chakravarti A. Cohen T, et al. Am J Med Genet. 1996 Oct 28;65(3):226-34. doi: 10.1002/(SICI)1096-8628(19961028)65:3<226::AID-AJMG11>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 9240749

2

A syndrome including thumb malformations, microcephaly, short stature, and hypogonadism.

Zlotogora J, Dagan J, Ganen A, Abu-Libdeh M, Ben-Neriah Z, Cohen T. Zlotogora J, et al. Among authors: cohen t. J Med Genet. 1997 Oct;34(10):813-6. doi: 10.1136/jmg.34.10.813. J Med Genet. 1997. PMID: 9350812 Free PMC article.

3

Familial hydrocephalus of prenatal onset.

Zlotogora J, Sagi M, Cohen T. Zlotogora J, et al. Among authors: cohen t. Am J Med Genet. 1994 Jan 15;49(2):202-4. doi: 10.1002/ajmg.1320490208. Am J Med Genet. 1994. PMID: 8116668

4

Estimated number of loci for autosomal recessive severe nerve deafness within the Israeli Jewish population, with implications for genetic counseling.

Brownstein Z, Friedlander Y, Peritz E, Cohen T. Brownstein Z, et al. Among authors: cohen t. Am J Med Genet. 1991 Dec 1;41(3):306-12. doi: 10.1002/ajmg.1320410309. Am J Med Genet. 1991. PMID: 1789284

5

Syndrome of brittle cornea, blue sclera, and joint hyperextensibility.

Zlotogora J, BenEzra D, Cohen T, Cohen E. Zlotogora J, et al. Among authors: cohen e, cohen t. Am J Med Genet. 1990 Jul;36(3):269-72. doi: 10.1002/ajmg.1320360303. Am J Med Genet. 1990. PMID: 2363420

6

High frequency of congenital adrenal hyperplasia (classic 11 beta-hydroxylase deficiency) among Jews from Morocco.

Rösler A, Leiberman E, Cohen T. Rösler A, et al. Among authors: cohen t. Am J Med Genet. 1992 Apr 1;42(6):827-34. doi: 10.1002/ajmg.1320420617. Am J Med Genet. 1992. PMID: 1554023

7

Application of the Health Belief Model in a study on parents' intentions to utilize prenatal diagnosis of cleft lip and/or palate.

Sagi M, Shiloh S, Cohen T. Sagi M, et al. Among authors: cohen t. Am J Med Genet. 1992 Oct 1;44(3):326-33. doi: 10.1002/ajmg.1320440312. Am J Med Genet. 1992. PMID: 1488980

8

Myotonic dystrophy: molecular analysis of Israeli patients.

Abeliovich D, Lerer I, Pashut-Lavon I, Cohen T. Abeliovich D, et al. Among authors: cohen t. Biomed Pharmacother. 1994;48(8-9):373-80. doi: 10.1016/0753-3322(94)90054-x. Biomed Pharmacother. 1994. PMID: 7858174

9

Anorectal malformations and Down syndrome.

Zlotogora J, Abu-Dalu K, Lernau O, Sagi M, Voss R, Cohen T. Zlotogora J, et al. Among authors: cohen t. Am J Med Genet. 1989 Nov;34(3):330-1. doi: 10.1002/ajmg.1320340307. Am J Med Genet. 1989. PMID: 2531980

10

Screening for five mutations detects 97% of cystic fibrosis (CF) chromosomes and predicts a carrier frequency of 1:29 in the Jewish Ashkenazi population.

Abeliovich D, Lavon IP, Lerer I, Cohen T, Springer C, Avital A, Cutting GR. Abeliovich D, et al. Among authors: cohen t. Am J Hum Genet. 1992 Nov;51(5):951-6. Am J Hum Genet. 1992. PMID: 1384328 Free PMC article.

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