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J I Rotter

Showing results (51-60 of 214) with videos related to

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Lancet (London, England)|May 19, 1979
Genetic heterogeneity in peptic ulcerJ I Rotter, D L Rimoin, I M Samloff
Clinical 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 Conte
American 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 Rotter
Gut|October 1, 1988
Gastrin cell function in familial multiple endocrine neoplasia type IC B Lamers, J I Rotter, J B Jansen
Gut|February 1, 1986
Pepsinogen genetics and duodenal ulcer diseaseJ I Rotter, I M Samloff, G M Petersen
American 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.
Genetic Epidemiology|January 1, 1992
Two-locus mitochondrial and nuclear gene models for mitochondrial disordersX Bu, H Y Yang, M Shohat, 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.
Advances in Experimental Medicine and Biology|January 1, 1995
The gene for familial Mediterranean fever is mapped to 16p 13.3- p13.1 with evidence for homogeneityM Shohat, N Fischel-Ghodsian, J I Rotter, 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.
Pageof 22

Showing results (51-60 of 214) with videos related to

Sort By:
Pageof 22
Lancet (London, England)|May 19, 1979
Genetic heterogeneity in peptic ulcerJ I Rotter, D L Rimoin, I M Samloff
Clinical 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 Conte
American 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 Rotter
Gut|October 1, 1988
Gastrin cell function in familial multiple endocrine neoplasia type IC B Lamers, J I Rotter, J B Jansen
Gut|February 1, 1986
Pepsinogen genetics and duodenal ulcer diseaseJ I Rotter, I M Samloff, G M Petersen
American 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.
Genetic Epidemiology|January 1, 1992
Two-locus mitochondrial and nuclear gene models for mitochondrial disordersX Bu, H Y Yang, M Shohat, 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.
Advances in Experimental Medicine and Biology|January 1, 1995
The gene for familial Mediterranean fever is mapped to 16p 13.3- p13.1 with evidence for homogeneityM Shohat, N Fischel-Ghodsian, J I Rotter, 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.
Pageof 22