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American Journal of Human Genetics|September 1, 1984
Human chromosomal assignments for 14 argininosuccinate synthetase pseudogenes: cloned DNAs as reagents for cytogenetic analysisT S Su, R L Nussbaum, S Airhart, et al.
Human Genetics|October 1, 1990
Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reactionJ R Batanian, S A Ledbetter, R K Wolff, et al.
Prenatal Diagnosis|September 1, 1996
Cytogenetic and age-dependent risk factors associated with uniparental disomy 15W P Robinson, S Langlois, S Schuffenhauer, et al.
American Journal of Human Genetics|November 1, 1988
Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndromeP vanTuinen, W B Dobyns, D C Rich, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndromeN Matsumoto, D E David, E W Johnson, et al.
Journal of Medical Genetics|June 3, 1999
The face of Smith-Magenis syndrome: a subjective and objective studyJ E Allanson, F Greenberg, A C Smith
Evolution & Development|July 3, 2004
Evolution of regulatory elements producing a conserved gene expression pattern in CaenorhabditisXiaodong Wang, Jennifer F Greenberg, Helen M Chamberlin
American Journal of Medical Genetics|July 1, 1984
Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephalyW B Dobyns, R F Stratton, F Greenberg
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