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Prenatal Diagnosis|August 11, 2018
Diagnosis and outcome in nonhydropic fetal pleural effusionsDiana Wellesley, David T HowePrenatal Diagnosis|July 10, 2020
Exomphalos without other prenatally detected anomalies: Perinatal outcomes from 22 years of population-based dataRose Grover, Amanda L Collins, Diana WellesleyPrenatal Diagnosis|January 24, 2009
Parental attitude to participating in long-term follow-up studies of their children's health after in utero diagnosis of abnormalitiesLauren Ramsay, David T Howe, Diana WellesleyJournal of Pediatric Urology|November 4, 2008
Congenital hydronephrosis: prenatal diagnosis and epidemiology in EuropeEster Garne, Maria Loane, Diana Wellesley, et al.BMJ (Clinical Research Ed.)|July 6, 2002
Retrospective audit of different antenatal screening policies for Down's syndrome in eight district general hospitals in one health regionDiana Wellesley, Tracy Boyle, John Barber, et al.Prenatal Diagnosis|January 9, 2016
What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysisShiri Shkedi-Rafid, Angela Fenwick, Sandi Dheensa, et al.Journal of Pediatric Orthopedics|February 27, 2003
Prenatal ultrasound: detection and diagnosis of limb abnormalitiesLiam Kevern, David Warwick, Diana Wellesley, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 16, 2017
Relationship between neonatal gastroschisis and maternal body mass index in a United Kingdom populationJoann Hale, Abigail Derbyshire, Alexander Taylor, et al.American Journal of Medical Genetics. Part A|June 24, 2004
SHOX mutations in a family and a fetus with Langer mesomelic dwarfismN Simon Thomas, Viv Maloney, Paul Bass, et al.Prenatal Diagnosis|April 13, 2021
Prenatal chromosome microarray: 'The UK experience'. A survey of reporting practices in UK genetic services (2012-2019)Jenny Patterson, Diana Wellesley, Sian Morgan, et al.Pageof 9