Shohat M - Search Results

1

Sensorineural deafness inherited as a tissue specific mitochondrial disorder.

Jaber L, Shohat M, Bu X, Fischel-Ghodsian N, Yang HY, Wang SJ, Rotter JI. Jaber L, et al. Among authors: shohat m. J Med Genet. 1992 Feb;29(2):86-90. doi: 10.1136/jmg.29.2.86. J Med Genet. 1992. PMID: 1613771 Free PMC article.

2

Biochemical characterization of a pedigree with mitochondrially inherited deafness.

Prezant RT, Shohat M, Jaber L, Pressman S, Fischel-Ghodsian N. Prezant RT, et al. Among authors: shohat m. Am J Med Genet. 1992 Nov 1;44(4):465-72. doi: 10.1002/ajmg.1320440416. Am J Med Genet. 1992. PMID: 1442889

3

The gene for familial Mediterranean fever in both Armenians and non-Ashkenazi Jews is linked to the alpha-globin complex on 16p: evidence for locus homogeneity.

Shohat M, Bu X, Shohat T, Fischel-Ghodsian N, Magal N, Nakamura Y, Schwabe AD, Schlezinger M, Danon Y, Rotter JI. Shohat M, et al. Among authors: shohat t. Am J Hum Genet. 1992 Dec;51(6):1349-54. Am J Hum Genet. 1992. PMID: 1463015 Free PMC article.

4

Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab community.

Jaber L, Merlob P, Bu X, Rotter JI, Shohat M. Jaber L, et al. Among authors: shohat m. Am J Med Genet. 1992 Sep 1;44(1):1-6. doi: 10.1002/ajmg.1320440102. Am J Med Genet. 1992. PMID: 1519638

5

Arthrogryposis multiplex congenita in an Arab kindred: update.

Jaber L, Weitz R, Bu X, Fischel-Ghodsian N, Rotter JI, Shohat M. Jaber L, et al. Among authors: shohat m. Am J Med Genet. 1995 Jan 30;55(3):331-4. doi: 10.1002/ajmg.1320550317. Am J Med Genet. 1995. PMID: 7726232

6

A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis.

Bu X, Shohat M, Jaber L, Rotter JI. Bu X, et al. Among authors: shohat m. Genet Epidemiol. 1993;10(1):3-15. doi: 10.1002/gepi.1370100102. Genet Epidemiol. 1993. PMID: 8472932

7

Consanguinity and common adult diseases in Israeli Arab communities.

Jaber L, Shohat T, Rotter JI, Shohat M. Jaber L, et al. Among authors: shohat t, shohat m. Am J Med Genet. 1997 Jun 27;70(4):346-8. doi: 10.1002/(sici)1096-8628(19970627)70:4<346::aid-ajmg2>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9182771

8

A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter.

Shohat M, Lotan R, Magal N, Shohat T, Fischel-Ghodsian N, Rotter JI, Jaber L. Shohat M, et al. Among authors: shohat t. Am J Hum Genet. 1997 Nov;61(5):1139-43. doi: 10.1086/301598. Am J Hum Genet. 1997. PMID: 9345093 Free PMC article.

9

Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation.

Bykhovskaya Y, Shohat M, Ehrenman K, Johnson D, Hamon M, Cantor RM, Aouizerat B, Bu X, Rotter JI, Jaber L, Fischel-Ghodsian N. Bykhovskaya Y, et al. Among authors: shohat m. Am J Med Genet. 1998 Jun 5;77(5):421-6. doi: 10.1002/(sici)1096-8628(19980605)77:5<421::aid-ajmg13>3.0.co;2-k. Am J Med Genet. 1998. PMID: 9632174

10

Candidate locus for a nuclear modifier gene for maternally inherited deafness.

Bykhovskaya Y, Estivill X, Taylor K, Hang T, Hamon M, Casano RA, Yang H, Rotter JI, Shohat M, Fischel-Ghodsian N. Bykhovskaya Y, et al. Among authors: shohat m. Am J Hum Genet. 2000 Jun;66(6):1905-10. doi: 10.1086/302914. Epub 2000 Apr 27. Am J Hum Genet. 2000. PMID: 10788333 Free PMC article.

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