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Nature Communications|October 27, 2019
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disordersM T Oetjens, M A Kelly, A C Sturm, et al.
Cancer Research|January 1, 1997
Deletion within the D17S34 locus in a primitive neuroectodermal tumorL Haataja, C Raffel, D H Ledbetter, et al.
Neurology|July 1, 1992
Causal heterogeneity in isolated lissencephalyW B Dobyns, E R Elias, A C Newlin, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1981
In vitro translation of hypoxanthine/guanine phosphoribosyltransferase mRNA: characterization of a mouse neuroblastoma cell line that has elevated levels of hypoxanthine/guanine phosphoribosyltransferase proteinD W Melton, D S Konecki, D H Ledbetter, et al.
American Journal of Medical Genetics|December 30, 1996
Robertsonian (15q;15q) translocation in a child with Angelman syndrome: evidence of uniparental disomyV Tonk, R A Schultz, S L Christian, et al.
Experimental Cell Research|January 1, 1991
Tumor suppression by chromosome 11 is not due to cellular senescenceY Ning, J W Shay, M Lovell, et al.
Biochemical and Biophysical Research Communications|November 27, 1985
The human apolipoprotein B-100 gene: a highly polymorphic gene that maps to the short arm of chromosome 2L Chan, P VanTuinen, D H Ledbetter, et al.
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