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American Journal of Medical Genetics|December 1, 1989
Linkage localization of Börjeson-Forssman-Lehmann syndromeK D Mathews, H H Ardinger, D Y Nishimura, et al.
Cancer Genetics and Cytogenetics|March 12, 1998
Detection of double minute chromosomes in a child with acute lymphoblastic leukemiaJ C Murray, D G Poplack, D H Mahoney, et al.
Medical Physics|June 1, 1994
Dosimetric problems at low monitor unit settings for scanned and scattering foil electron beamsI J Das, J C Harrington, S F Akber, et al.
Nucleic Acids Research|July 11, 1992
Construction of a human chromosome 4 YAC pool and analysis of artificial chromosome stabilityH M Sleister, K A Mills, S E Blackwell, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|August 11, 2000
Localization of dominantly inherited isolated triphalangeal thumb to chromosomal region 7q36M B Dobbs, F R Dietz, C A Gurnett, et al.
Journal of Pediatric Hematology/Oncology|July 24, 2001
Infantile cytomegalovirus-associated autoimmune hemolytic anemiaJ C Murray, J C Bernini, H L Bijou, et al.
European Journal of Epidemiology|April 29, 1998
The effect of follow-up on limiting non-participation bias in genetic epidemiologic investigationsP A Romitti, R G Munger, J C Murray, et al.
American Journal of Medical Genetics. Part A|September 21, 2004
Mutations in PITX2 may contribute to cases of omphalocele and VATER-like syndromesL A Katz, R E Schultz, E V Semina, et al.
Journal of Leukocyte Biology|February 26, 2004
Endothelial monocyte-activating polypeptide-II (EMAP-II): a novel inducer of lymphocyte apoptosisJ C Murray, Y M Heng, P Symonds, et al.
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