Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 2, 2002
Congenital hypothyroidism with Prader-Willi syndromeCarron Sher, Tzvi Bistritzer, Gad Reisler, et al.
American Journal of Medical Genetics. Part A|July 3, 2003
Factors affecting performance of prenatal genetic testing by Israeli Jewish womenCarron Sher, Orly Romano-Zelekha, Manfred S Green, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 14, 2003
A founder COL17A1 splice site mutation leading to generalized atrophic benign epidermolysis bullosa in an extended inbred Palestinian family from IsraelNeil Vincent Whittock, Carron Sher, Isaac Gold, et al.
Archives of Neurology|March 15, 2006
De novo occurrence of novel SPG3A/atlastin mutation presenting as cerebral palsyShirley Rainier, Carron Sher, Orit Reish, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|April 1, 2004
Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXXOrit Reish, Todd Berryman, Thomas R Cunningham, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 2, 2003
Asynchronous replication of biallelically expressed loci: a new phenomenon in Turner syndromeOrit Reish, Ron Gal, Elena Gaber, et al.
Cancer Genetics and Cytogenetics|June 5, 2003
Modified allelic replication in lymphocytes of patients with neurofibromatosis type 1Orit Reish, Ana Orlovski, Maya Mashevitz, et al.
Pageof 1