Embryology of neural tube defects: information provided by associated malformations
A.-S. Cabaret(Université de Rennes), P. Poulain, Philippe Loget(Hôpital Pontchaillou), S. Odent(CIC Rennes)
Cited by 15
Related Papers
Mutation update for the <i>CSB</i> / <i>ERCC6</i> and <i>CSA</i> / <i>ERCC8</i> genes involved in Cockayne syndrome
|Human Mutation|2009|231
ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder
|The American Journal of Human Genetics|2017|141
Perinatal‐lethal Gaucher disease
|American Journal of Medical Genetics Part A|2003|127
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects
|Human Molecular Genetics|2013|112
Severe Prenatal Renal Anomalies Associated with Mutations in HNF1B or PAX2 Genes
|Clinical Journal of the American Society of Nephrology|2013|110