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Archives of Disease in Childhood. Fetal and Neonatal Edition|August 14, 2014
Epidemiology of partial urorectal septum malformation sequence (or 'persistent cloaca'): a population-based study in seven regions of England and Wales, 1985-2010Peter W G Tennant, Svetlana V Glinianaia, Diana Wellesley, et al.
Emerging Themes in Epidemiology|July 10, 2007
Geographic variation and localised clustering of congenital anomalies in Great BritainBen G Armstrong, Helen Dolk, Sam Pattenden, et al.
Environment International|June 25, 2019
Risk of congenital anomalies near municipal waste incinerators in England and Scotland: Retrospective population-based cohort studyBrandon Parkes, Anna L Hansell, Rebecca E Ghosh, et al.
BMC Medical Genomics|February 27, 2021
A hemizygous mutation in the FOXP3 gene (IPEX syndrome) resulting in recurrent X-linked fetal hydrops: a case reportPanicos Shangaris, Alison Ho, Andreas Marnerides, et al.
Environmental Health Perspectives|February 22, 2008
Chlorination disinfection by-products and risk of congenital anomalies in England and WalesMark J Nieuwenhuijsen, Mireille B Toledano, James Bennett, et al.
Archives of Disease in Childhood|July 27, 2010
Autism, language and communication in children with sex chromosome trisomiesDorothy V M Bishop, Patricia A Jacobs, Katherine Lachlan, et al.
Pediatric Nephrology (Berlin, Germany)|May 14, 2025
Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninismLuisa Marsili, Matthieu Mantecon, Christelle Arrondel, et al.
Prenatal Diagnosis|June 12, 2014
Prenatal diagnosis and epidemiology of multicystic kidney dysplasia in EuropeLouise Winding, Maria Loane, Diana Wellesley, et al.
Orphanet Journal of Rare Diseases|February 18, 2025
Health outcomes and drug utilisation in children with Noonan syndrome: a European cohort studyMichele Santoro, Ingeborg Barisic, Alessio Coi, et al.
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