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Lancet (London, England)
|
May 19, 1979
Genetic heterogeneity in peptic ulcer
J 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 enteropathy
H 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 disorders
F L Wong, R M Cantor, J I Rotter
Gut
|
October 1, 1988
Gastrin cell function in familial multiple endocrine neoplasia type I
C B Lamers, J I Rotter, J B Jansen
Gut
|
February 1, 1986
Pepsinogen genetics and duodenal ulcer disease
J 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 determination
Y Wang, Y S Rabinowitz, J I Rotter, et al.
Genetic Epidemiology
|
January 1, 1992
Two-locus mitochondrial and nuclear gene models for mitochondrial disorders
X 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 community
L 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 homogeneity
M 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.
Page
of 22
Search research articles
Search
Showing results (51-60 of 214) with videos related to
Sort By:
Page
of 22
Lancet (London, England)
|
May 19, 1979
Genetic heterogeneity in peptic ulcer
J 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 enteropathy
H 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 disorders
F L Wong, R M Cantor, J I Rotter
Gut
|
October 1, 1988
Gastrin cell function in familial multiple endocrine neoplasia type I
C B Lamers, J I Rotter, J B Jansen
Gut
|
February 1, 1986
Pepsinogen genetics and duodenal ulcer disease
J 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 determination
Y Wang, Y S Rabinowitz, J I Rotter, et al.
Genetic Epidemiology
|
January 1, 1992
Two-locus mitochondrial and nuclear gene models for mitochondrial disorders
X 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 community
L 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 homogeneity
M 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.
Page
of 22