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The Nursing Clinics of North America|August 25, 2000
Genetic testing and screening in pediatric populationsJ Davis, D Krasnewich, J M PuckCytogenetics and Cell Genetics|January 1, 1996
Gene localization and syntenic mapping by FISH in the dogA S Dutra, E Mignot, J M PuckAmerican Journal of Medical Genetics|June 28, 2001
Sib understanding of genetics and attitudes toward carrier testing for X-linked severe combined immunodeficiencyJ H Fanos, J Davis, J M PuckHuman Genetics|May 1, 1997
Carrier and prenatal diagnosis of X-linked severe combined immunodeficiency: mutation detection methods and utilizationJ M Puck, L Middelton, A E PepperGene Therapy|August 5, 2016
The long terminal repeat negative control region is a critical element for insertional oncogenesis after gene transfer into hematopoietic progenitors with Moloney murine leukemia viral vectorsY Ikawa, T Uchiyama, G J Jagadeesh, et al.American Journal of Human Genetics|July 1, 1993
Refinement of linkage of human severe combined immunodeficiency (SCIDX1) to polymorphic markers in Xq13J M Puck, M E Conley, L C BaileyGenomics|January 1, 1993
Twelve new polymorphic microsatellites on human chromosome 22J C Porter, K T Ram, J M PuckThe Journal of Clinical Investigation|May 1, 1987
Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivationJ M Puck, R L Nussbaum, M E ConleyThe Journal of Experimental Medicine|October 1, 1981
Antigen presentation to human T lymphocytes. I. Different requirements for stimulation by hapten-modified cells vs. cell sonicatesS L Abramson, J M Puck, R R RichAmerican Journal of Human Genetics|April 1, 1992
Maximum-likelihood analysis of human T-cell X chromosome inactivation patterns: normal women versus carriers of X-linked severe combined immunodeficiencyJ M Puck, C C Stewart, R L NussbaumPageof 14