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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 JansenBritish Journal of Cancer|June 27, 2002
Reduced risk of synovial sarcoma in females: X-chromosome inactivation?X Bu, L Bernstein, R K BrynesAmerican Journal of Medical Genetics|August 22, 2000
Genetic epidemiological study of keratoconus: evidence for major gene determinationY Wang, Y S Rabinowitz, J I Rotter, et al.Experimental Hematology|February 1, 1996
Erythropoietin stimulates phosphorylation of eIF-4E and identification of a 37-kD phosphoprotein that binds mRNA caps in erythroblastsX Bu, M C Bondurant, C H HagedornZhonghua Er Bi Yan Hou Ke Za Zhi|May 24, 2003
[A preliminary study of a hearing screening model for newborn]Z Liu, X Bu, G Xing, et al.Pageof 25