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Journal of Clinical Microbiology|August 1, 1992
Immunoglobulin A (IgA) and IgG serum antibodies to mycobacterial antigens in Crohn's disease patients and their relativesL G Wayne, D Hollander, B Anderson, et al.
Human Heredity|May 1, 1995
Polymorphic gene markers in Mexican-Americans residing in southern CaliforniaT Shohat, S J Shaw, R S Sparkes, et al.
Gastroenterology|November 1, 1989
Lack of an association between polymorphisms of the T-cell receptor alpha-chain and ulcerative colitisL M Randolph, H Toyoda, C K McElree, et al.
American Journal of Human Genetics|November 5, 1997
A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qterM Shohat, R Lotan, N Magal, et al.
Journal of Medical Genetics|November 14, 1997
Spondylo-mesomelic-acrodysplasia with joint dislocations and severe combined immunodeficiency: a newly recognised immuno-osseous dysplasiaA Castriota-Scanderbeg, R Mingarelli, G Caramia, et al.
American Journal of Medical Genetics|January 20, 1997
The Pointer syndrome: a new syndrome with skeletal abnormalities, camptodactyly, facial anomalies, and feeding difficultiesA H Huq, R M Braverman, F Greenberg, et al.
The British Journal of Ophthalmology|July 1, 1996
Videokeratography database of normal human corneasY S Rabinowitz, H Yang, Y Brickman, et al.
American Journal of Medical Genetics|July 1, 1985
Chondrodysplasia punctata in an infant with duplication 16p due to a 7;16 translocationA G Hunter, D L Rimoin, U M Koch, et al.
The Journal of Biological Chemistry|November 5, 1992
An amino acid substitution (Gly853-->Glu) in the collagen alpha 1(II) chain produces hypochondrogenesisR Bogaert, G E Tiller, M A Weis, et al.
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