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BMC Neurology|January 15, 2020
Childhood neurodegeneration associated with a specific UBTF variant: a new case report and review of the literatureFilipa Bastos, Mathieu Quinodoz, Marie-Claude Addor, et al.
American Journal of Medical Genetics. Part A|July 17, 2008
Subtelomeric 6p deletion: clinical and array-CGH characterization in two patientsDanielle Martinet, Isabel Filges, Nathalie Besuchet Schmutz, et al.
BMJ (Clinical Research Ed.)|June 27, 2018
Metformin exposure in first trimester of pregnancy and risk of all or specific congenital anomalies: exploratory case-control studyJoanne E Given, Maria Loane, Ester Garne, et al.
Prenatal Diagnosis|June 12, 2014
Prenatal diagnosis and epidemiology of multicystic kidney dysplasia in EuropeLouise Winding, Maria Loane, Diana Wellesley, et al.
Journal of Clinical Psychopharmacology|December 30, 2022
Reproductive Safety of Trazodone After Maternal Exposure in Early Pregnancy: A Comparative ENTIS Cohort StudyKim Dao, Svetlana Shechtman, Orna Diav-Citrin, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|June 24, 2019
Methadone, Pierre Robin sequence and other congenital anomalies: case-control studyBrian Cleary, Maria Loane, Marie-Claude Addor, et al.
Prenatal Diagnosis|November 27, 2004
Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 regions of EuropeEster Garne, Maria Loane, Catherine de Vigan, et al.
European Journal of Human Genetics : EJHG|January 12, 2012
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in EuropeDiana Wellesley, Helen Dolk, Patricia A Boyd, et al.
Environmental Health Perspectives|March 5, 2004
Toward the effective surveillance of hypospadiasHelen Dolk, Martine Vrijheid, John E S Scott, et al.
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