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Birth Defects Research. Part A, Clinical and Molecular Teratology|November 25, 2003
Selection of normalizer genes in conducting relative gene expression analysis of embryosQin J Zhang, Antony Chadderton, Robert L Clark, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 25, 2003
Genotype frequencies and linkage disequilibrium in the CEPH human diversity panel for variants in folate pathway genes MTHFR, MTHFD, MTRR, RFC1, and GCP2Min Shi, Diana Caprau, Paul Romitti, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 25, 2003
Association of congenital diaphragmatic hernia with limb-reduction defectsMarieke F van Dooren, Alice S Brooks, Dick Tibboel, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 25, 2003
Joint laxity and the risk of clubfootAndrew F Olshan, Jane C Schroeder, Beth W Alderman, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 28, 2004
Multiple congenital anomalies associated with in utero exposure of phenytoin: possible hypoxic ischemic mechanism?Helen M Lyon, Lewis B Holmes, Taosheng Huang
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 28, 2004
Trend in prevalence of neural tube defects in QuebecPhilippe De Wals, Ira David Rusen, Nora S Lee, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 28, 2004
Timetable for intestinal rotation in staged human embryos and fetusesWon Kyu Kim, Hyun Kim, Dae Ho Ahn, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 28, 2004
Fetal bilateral renal agenesis, phocomelia, and single umbilical artery associated with cocaine abuse in early pregnancyMaki Kashiwagi, Rabih Chaoui, Thomas Stallmach, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 28, 2004
Developmental immunotoxicity of lead: impact on thymic functionJi-Eun Lee, Rodney R Dietert
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 28, 2004
Persistent Mullerian duct syndrome caused by both a 27-bp deletion and a novel splice mutation in the MIS type II receptor geneMakiko Hoshiya, Benjamin P Christian, William J Cromie, et al.
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