Showing results (1-10 of 591) with videos related to
Sort By:
Pageof 60
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1988
Klippel-Feil anomaly with sacral agenesis: an additional subtype, type IVA Raas-Rothschild, R M Goodman, M Grunbaum, et al.Journal of Craniofacial Genetics and Developmental Biology|January 1, 1989
Newly recognized ectrodactyly/deafness syndromeA Raas-Rothschild, A Aviram, T Ben-Ami, et al.Clinical Genetics|August 1, 1990
Megalocornea, macrocephaly, mental and motor retardation (MMMM)M Frydman, M Berkenstadt, A Raas-Rothschild, et al.Clinical Genetics|January 1, 1990
Skin mastocytosis with short stature, conductive hearing loss and microtia: a new syndromeB Wolach, A Raas-Rothschild, A Metzker, et al.The Pediatric Infectious Disease Journal|November 1, 1992
Oral ciprofloxacin in the management of chronic suppurative otitis media without cholesteatoma in children: preliminary experience in 21 childrenR Lang, S Goshen, A Raas-Rothschild, et al.American Journal of Medical Genetics|March 4, 2000
Giant congenital aortic aneurysm with cleft sternum, supraumbilical raphé, and hemangiomatosis: report and reviewA Raas-Rothschild, A Nir, R Gillis, et al.Biochemical Medicine and Metabolic Biology|June 1, 1994
Mutations of the hexosaminidase A gene in Ashkenazi and non-Ashkenazi JewsL Peleg, M Karpati, E Gazit, et al.Journal of Medical Genetics|June 1, 1981
Anal atresia and the Klein-Waardenburg syndromeJ Nutman, I Nissenkorn, I Varsano, et al.European Journal of Human Genetics : EJHG|June 3, 1999
Mucolipidosis type IV: the origin of the disease in the Ashkenazi Jewish populationA Raas-Rothschild, R Bargal, S DellaPergola, et al.Dermatologica|January 1, 1990
Subcutaneous fat necrosis with thrombocytopenia in a newborn infantB Wolach, A Raas-Rothschild, R Vogel, et al.Pageof 60