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American Journal of Medical Genetics|June 27, 1997
Consanguinity and common adult diseases in Israeli Arab communitiesL Jaber, T Shohat, J I Rotter, et al.Clinical Genetics|February 1, 1985
Disease risk estimates from marker association data. Application to individuals at risk for hemochromatosisH J Lin, W J Conte, J I RotterAmerican Journal of Human Genetics|March 1, 1982
Evidence for recessive and against dominant inheritance at the HLA-"linked" locus in coeliac diseaseD A Greenberg, S E Hodge, J I RotterClinical Genetics|September 1, 1985
Use of HLA marker associations and HLA haplotype linkage to estimate disease risks in families with gluten-sensitive enteropathyH J Lin, J I Rotter, W J ConteAmerican Journal of Human Genetics|July 1, 1986
Sample-size considerations and strategies for linkage analysis in autosomal recessive disordersF L Wong, R M Cantor, J I RotterGut|October 1, 1988
Gastrin cell function in familial multiple endocrine neoplasia type IC B Lamers, J I Rotter, J B JansenUltrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 28, 2003
Use of three-dimensional ultrasound imaging in the diagnosis of prenatal-onset skeletal dysplasiasD Krakow, J Williams, M Poehl, et al.Proceedings of the National Academy of Sciences of the United States of America|May 1, 1990
Tandem duplication within a type II collagen gene (COL2A1) exon in an individual with spondyloepiphyseal dysplasiaG E Tiller, D L Rimoin, L W Murray, et al.The Journal of Pediatrics|May 1, 1979
Further heterogeneity within lethal neonatal short-limbed dwarfism: the platyspondylic typesW A Horton, D L Rimoin, D W Hollister, et al.American Journal of Optometry and Physiological Optics|February 1, 1980
Optometric screening in achondroplasia, diastrophic dysplasia, and spondyloepiphyseal dysplasia congenitaJ R Griffin, J E Ault, D O Sillence, et al.Pageof 42