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M Shohat

Showing results (91-100 of 190) with videos related to

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American Journal of Medical Genetics|March 17, 1997
Agenesis of the corpus callosum in a mother and sonD Inbar, G J Halpern, R Weitz, et al.
American Journal of Medical Genetics|June 1, 1993
New form of spondyloepimetaphyseal dysplasia (SEMD) in Jewish family of Iraqi originM Shohat, R Lachman, R Carmi, et al.
American Journal of Medical Genetics|September 1, 1992
Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab communityL Jaber, P Merlob, X Bu, et al.
Pediatric Radiology|January 1, 1991
Perinatal lethal hypophosphatasia; clinical, radiologic and morphologic findingsM Shohat, D L Rimoin, H E Gruber, et al.
American Journal of Medical Genetics|August 8, 1997
Correlation between the incidence of myotonic dystrophy in different groups in Israel and the number of CTG trinucleotide repeats in the myotonin geneR Mor-Cohen, N Magal, N Gadoth, et al.
Archives of Disease in Childhood|January 1, 1987
Childhood asthma and growth outcomeM Shohat, T Shohat, R Kedem, et al.
American Journal of Medical Genetics|June 26, 2001
Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblingsY Senecky, G J Halpern, D Inbar, et al.
American Journal of Medical Genetics|December 31, 1997
Further delineation of cerebro-osteo-nephrosis syndromeY Udler, G J Halpern, C Sher, et al.
American Journal of Medical Genetics|October 1, 1989
Hypothesis: familial Mediterranean fever--a genetic disorder of the lipocortin family?M Shohat, J R Korenberg, A D Schwabe, et al.
American Journal of Medical Genetics|March 21, 1998
Syndrome of alopecia totalis and 17b-hydroxysteroid dehydrogenase deficiencyA Kauschansky, M Shohat, M Frydman, et al.
Pageof 19

Showing results (91-100 of 190) with videos related to

Sort By:
Pageof 19
American Journal of Medical Genetics|March 17, 1997
Agenesis of the corpus callosum in a mother and sonD Inbar, G J Halpern, R Weitz, et al.
American Journal of Medical Genetics|June 1, 1993
New form of spondyloepimetaphyseal dysplasia (SEMD) in Jewish family of Iraqi originM Shohat, R Lachman, R Carmi, et al.
American Journal of Medical Genetics|September 1, 1992
Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab communityL Jaber, P Merlob, X Bu, et al.
Pediatric Radiology|January 1, 1991
Perinatal lethal hypophosphatasia; clinical, radiologic and morphologic findingsM Shohat, D L Rimoin, H E Gruber, et al.
American Journal of Medical Genetics|August 8, 1997
Correlation between the incidence of myotonic dystrophy in different groups in Israel and the number of CTG trinucleotide repeats in the myotonin geneR Mor-Cohen, N Magal, N Gadoth, et al.
Archives of Disease in Childhood|January 1, 1987
Childhood asthma and growth outcomeM Shohat, T Shohat, R Kedem, et al.
American Journal of Medical Genetics|June 26, 2001
Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblingsY Senecky, G J Halpern, D Inbar, et al.
American Journal of Medical Genetics|December 31, 1997
Further delineation of cerebro-osteo-nephrosis syndromeY Udler, G J Halpern, C Sher, et al.
American Journal of Medical Genetics|October 1, 1989
Hypothesis: familial Mediterranean fever--a genetic disorder of the lipocortin family?M Shohat, J R Korenberg, A D Schwabe, et al.
American Journal of Medical Genetics|March 21, 1998
Syndrome of alopecia totalis and 17b-hydroxysteroid dehydrogenase deficiencyA Kauschansky, M Shohat, M Frydman, et al.
Pageof 19