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Archives of Disease in Childhood. Fetal and Neonatal Edition|November 21, 2014
Epidemiology of congenital diaphragmatic hernia in Europe: a register-based studyMark R McGivern, Kate E Best, Judith Rankin, et al.American Journal of Medical Genetics. Part A|July 12, 2019
Epidemiology of achondroplasia: A population-based study in EuropeAlessio Coi, Michele Santoro, Ester Garne, et al.BMJ (Clinical Research Ed.)|September 15, 2016
Prevalence of microcephaly in Europe: population based studyJoan K Morris, Judith Rankin, Ester Garne, et al.Paediatric and Perinatal Epidemiology|June 16, 2021
Epidemiology of Pierre-Robin sequence in Europe: A population-based EUROCAT studyMichele Santoro, Alessio Coi, Ingeborg Barišić, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|October 27, 2022
Epidemiology of aplasia cutis congenita: A population-based study in EuropeAlessio Coi, Ingeborg Barisic, Ester Garne, et al.Paediatric and Perinatal Epidemiology|June 8, 2022
Temporal and geographical variations in survival of children born with congenital anomalies in Europe: A multi-registry cohort studyMichele Santoro, Alessio Coi, Anna Pierini, et al.Frontiers in Pediatrics|July 12, 2021
Prevention of Neural Tube Defects in Europe: A Public Health FailureJoan K Morris, Marie-Claude Addor, Elisa Ballardini, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|March 8, 2011
Paper 6: EUROCAT member registries: organization and activitiesRuth Greenlees, Amanda Neville, Marie-Claude Addor, et al.American Journal of Medical Genetics. Part A|December 30, 2022
Amniotic band syndrome and limb body wall complex in Europe 1980-2019Jorieke E H Bergman, Ingeborg Barišić, Marie-Claude Addor, et al.Journal of Medical Genetics|March 5, 2013
Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvementMiriam Schmidts, Heleen H Arts, Ernie M H F Bongers, et al.Pageof 9