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American Journal of Human Genetics|August 10, 2000
A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21D H Cohn, T Shohat, M Yahav, et al.
Ophthalmology|November 1, 1986
Long-term results of cryotherapy for active stages of retinopathy of prematurityI Ben-Sira, I Nissenkorn, D Weinberger, et al.
American Journal of Human Genetics|November 5, 1997
A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qterM Shohat, R Lotan, N Magal, et al.
American Journal of Medical Genetics|March 1, 1993
Hearing loss and temporal bone structure in achondroplasiaM Shohat, E Flaum, S R Cobb, et al.
American Journal of Medical Genetics|June 27, 2000
Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotesV Drasinover, S Ehrlich, N Magal, et al.
The Israel Medical Association Journal : IMAJ|January 17, 2002
Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studiesT Ilan, T Shohat, A Tobar, et al.
International Journal of Biometeorology|November 1, 1995
Solar activity cycle and the incidence of foetal chromosome abnormalities detected at prenatal diagnosisG J Halpern, E G Stoupel, G Barkai, et al.
Human Mutation|May 29, 1998
Assessment of pyrin gene mutations in Turks with familial Mediterranean fever (FMF)X Chen, N Fischel-Ghodsian, A Cercek, et al.
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