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BJOG : an International Journal of Obstetrics and Gynaecology|February 7, 2013
Trends in the prevalence, risk and pregnancy outcome of multiple births with congenital anomaly: a registry-based study in 14 European countries 1984-2007B Boyle, R McConkey, E Garne, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|April 12, 2013
Anorectal malformations and pregnancy-related disorders: a registry-based case-control study in 17 European regionsC H W Wijers, I A L M van Rooij, M K Bakker, et al.
American Journal of Medical Genetics. Part A|May 13, 2017
Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotypeEmma M Wade, Zandra A Jenkins, Philip B Daniel, et al.
Molecular Syndromology|November 4, 2010
IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS SignL Desmyter, M Ghassibe, N Revencu, et al.
Birth Defects Research|January 31, 2025
Risk of Congenital Ocular Anomaly After Prenatal Exposure to Medications: A EUROmediCAT StudyE-A Cifuentes, A Beau, A Caillet, et al.
Clinical Genetics|October 21, 2016
Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?S El Chehadeh, R Touraine, F Prieur, et al.
Clinical Genetics|March 20, 2013
Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disabilityP Callier, B Aral, N Hanna, et al.
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