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American Journal of Medical Genetics. Part A|December 21, 2002
Risk perception of participants in a family-based genetic screening program on familial hypercholesterolemiaM C van Maarle, M E A Stouthard, G J BonselAmerican Journal of Medical Genetics. Part A|December 21, 2002
Lack of association between Y chromosome haplogroups and male infertility in Japanese menCláudia M B Carvalho, Masato Fujisawa, Toshiro Shirakawa, et al.American Journal of Medical Genetics. Part A|September 2, 2003
A gene for nonsyndromic X-linked mental retardation (MRX77) maps to Xq12-Xq21.33Carolina Sismani, Maria Syrrou, Kyproula Christodoulou, et al.American Journal of Medical Genetics. Part A|September 2, 2003
Relative prevalence of malformations at birth among different religious communities in IsraelJoël Zlotogora, Ziona Haklai, Naama Rotem, et al.American Journal of Medical Genetics. Part A|September 2, 2003
Rib defects in patterns of multiple malformations: a retrospective review and phenotypic analysis of 47 casesDuangrurdee Wattanasirichaigoon, Chitra Prasad, Gretchen Schneider, et al.American Journal of Medical Genetics. Part A|September 2, 2003
Patient with Kabuki syndrome and acute leukemiaSabine Scherer, Ursel Theile, Vera Beyer, et al.American Journal of Medical Genetics. Part A|July 3, 2003
Factors affecting performance of prenatal genetic testing by Israeli Jewish womenCarron Sher, Orly Romano-Zelekha, Manfred S Green, et al.American Journal of Medical Genetics. Part A|August 19, 2003
Methionine synthase (MTR) 2756 (A --> G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndromePaolo Bosco, Rosa-Maria Guéant-Rodriguez, Guido Anello, et al.American Journal of Medical Genetics. Part A|August 19, 2003
Vasomotor instability in neonates with chromosome 22q11 deletion syndromeVandana Shashi, Margaret N Berry, Michael H HinesAmerican Journal of Medical Genetics. Part A|August 19, 2003
Sequence-based, in situ detection of chromosomal abnormalities at high resolutionJoan H M Knoll, Peter K RoganPageof 928