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Birth Defects Research. Part A, Clinical and Molecular Teratology|October 5, 2010
Studies with Wnt genes and nonsyndromic cleft lip and palateRenato Menezes, Ariadne Letra, Ana H Kim, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|October 5, 2010
Risk of birth defects increased in multiple birthsXiao-Hui Zhang, Li-Qian Qiu, Jiang-Ping HuangBirth Defects Research. Part A, Clinical and Molecular Teratology|October 5, 2010
Maternal polymorphisms in folic acid metabolic genes are associated with nonsyndromic cleft lip and/or palate in the Brazilian populationAndreia Bufalino, Lívia Máris Ribeiro Paranaíba, Sibele Nascimento de Aquino, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|September 16, 2010
The role of CYP26 enzymes in defining appropriate retinoic acid exposure during embryogenesisTracie Pennimpede, Don A Cameron, Glenn A MacLean, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|February 14, 2009
Measurements of birth defect prevalence: which is most useful as a comparator group for pharmaceutical pregnancy registries?Angela Scheuerle, Vani X Vannappagari, Mary K MillerBirth Defects Research. Part A, Clinical and Molecular Teratology|February 14, 2009
Segregation analysis of cleft lip with or without cleft palate in the First Nations (Amerindian) people of British Columbia and review of isolated cleft palate etiologiesR Brian Lowry, Candice Y Johnson, France Gagnon, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|February 14, 2009
Methylenetetrahydrofolate reductase deficiency and low dietary folate increase embryonic delay and placental abnormalities in miceLaura Pickell, Deqiang Li, Katharine Brown, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|August 1, 2009
Socioeconomic measures, orofacial clefts, and conotruncal heart defects in CaliforniaSuzan L Carmichael, Chen Ma, Gary M ShawBirth Defects Research. Part A, Clinical and Molecular Teratology|August 1, 2009
Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndromeCarrie L Heike, Jacqueline R Starr, Mark J Rieder, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|May 15, 2009
The long arms of anencephaly: A refutationMason BarrPageof 126