The modes of inheritance of insulin-dependent diabetes mellitus or the genetics of IDDM, no longer a nightmare but still a headache.

por Rotter, J I
Publicado 1981

Epstein-Barr virus transformation of cryopreserved lymphocytes: prolonged experience with technique.

por Pressman, S, Rotter, J I
Publicado 1991

X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation.

por Bu, X D, Rotter, J I
Publicado 1991

Genetics of diabetes.

por Rotter, J I, Rimoin, D L
Publicado 1983

The use of association data to identify family members at high risk for marker-linked diseases.

por Conte, W J, Rotter, J I
Publicado 1984

Sample-size calculations in segregation analysis.

por Wong, F L, Rotter, J I
Publicado 1984

Cost-effective sib-pair designs in the mapping of quantitative-trait loci.

por Zhao, H, Zhang, H, Rotter, J I
Publicado 1997

Evidence for recessive and against dominant inheritance at the HLA-"linked" locus in coeliac disease.

por Greenberg, D A, Hodge, S E, Rotter, J I
Publicado 1982

Pepsinogen genetics and duodenal ulcer disease.

por Rotter, J I, Samloff, I M, Petersen, G M
Publicado 1986

Gastrin cell function in familial multiple endocrine neoplasia type I.

por Lamers, C B, Rotter, J I, Jansen, J B
Publicado 1988

Sample-size considerations and strategies for linkage analysis in autosomal recessive disorders.

por Wong, F L, Cantor, R M, Rotter, J I
Publicado 1986

Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion.

por Blumberg, B D, Shulkin, J D, Rotter, J I, Mohandas, T, Kaback, M M
Publicado 1982

Videokeratography database of normal human corneas.

por Rabinowitz, Y. S., Yang, H., Brickman, Y., Akkina, J., Riley, C., Rotter, J. I., Elashoff, J.
Publicado 1996

Familial empirical risks for inflammatory bowel disease: differences between Jews and non-Jews.

por Yang, H, McElree, C, Roth, M P, Shanahan, F, Targan, S R, Rotter, J I
Publicado 1993

HLA-dependent GM effects in insulin-dependent diabetes: evidence from pairs of affected siblings.

por Field, L L, Dizier, M H, Anderson, C E, Spence, M A, Rotter, J I
Publicado 1986

A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter.

por Shohat, M, Lotan, R, Magal, N, Shohat, T, Fischel-Ghodsian, N, Rotter, J I, Jaber, L
Publicado 1997

Genetic variation in lipoprotein (a) levels in families enriched for coronary artery disease is determined almost entirely by the apolipoprotein (a) gene locus.

por DeMeester, C A, Bu, X, Gray, R J, Lusis, A J, Rotter, J I
Publicado 1995

Immunoglobulin A (IgA) and IgG serum antibodies to mycobacterial antigens in Crohn's disease patients and their relatives.

por Wayne, L G, Hollander, D, Anderson, B, Sramek, H A, Vadheim, C M, Rotter, J I
Publicado 1992

Ulcerative colitis: a genetically heterogeneous disorder defined by genetic (HLA class II) and subclinical (antineutrophil cytoplasmic antibodies) markers.

por Yang, H, Rotter, J I, Toyoda, H, Landers, C, Tyran, D, McElree, C K, Targan, S R
Publicado 1993

Sensorineural deafness inherited as a tissue specific mitochondrial disorder.

por Jaber, L, Shohat, M, Bu, X, Fischel-Ghodsian, N, Yang, H Y, Wang, S J, Rotter, J I
Publicado 1992