au.\*:("WELLESLEY, Diana")
Results 1 to 10 of 10
Selection :
Prenatal diagnosis of chromosomal imbalancesWELLESLEY, Diana G; LUCASSEN, Anneke.Archives of disease in childhood. Fetal and neonatal edition. 2014, Vol 99, Num 4, issn 1359-2998, F338-F341Article
Parental attitude to participating in long-term follow-up studies of their children's health after in utero diagnosis of abnormalitiesRAMSAY, Lauren; HOWE, David T; WELLESLEY, Diana et al.Prenatal diagnosis. 2009, Vol 29, Num 3, pp 207-212, issn 0197-3851, 6 p.Article
Fetal renal anomalies and genetic syndromesWELLESLEY, Diana; HOWE, David T.Prenatal diagnosis. 2001, Vol 21, Num 11, pp 992-1003, issn 0197-3851Article
Retrospective audit of different antenatal screening policies for Down's syndrome in eight district general hospitals in one health regionWELLESLEY, Diana; BOYLE, Tracy; BARBER, John et al.BMJ. British medical journal (International ed.). 2002, Vol 325, Num 7354, pp 15-17, issn 0959-8146Article
Prenatal ultrasound: Detection and diagnosis of limb abnormalitiesKEVERN, Liam; WARWICK, David; WELLESLEY, Diana et al.Journal of pediatric orthopedics. 2003, Vol 23, Num 2, pp 251-253, issn 0271-6798, 3 p.Article
SHOX mutations in a family and a fetus with langer mesomelic dwarfismTHOMAS, N. Simon; MALONEY, Viv; BASS, Paul et al.American journal of medical genetics. 2004, Vol 128A, Num 2, pp 179-184, issn 0148-7299, 6 p.Article
Descriptive Epidemiology of Cornelia de Lange Syndrome in EuropeBARISIC, Ingeborg; TOKIC, Visnja; LOANE, Maria et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 1, pp 51-59, issn 1552-4825, 9 p.Article
Epidemiology of partial urorectal septum malformation sequence (or 'persistent cloaca'): a population-based study in seven regions of England and Wales, 1985-2010TENNANT, Peter W. G; GLINIANAIA, Svetlana V; WELLESLEY, Diana et al.Archives of disease in childhood. Fetal and neonatal edition. 2014, Vol 99, Num 5, issn 1359-2998, F413-F418Article
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in EuropeWELLESLEY, Diana; DOLK, Helen; MULLANEY, Carmel et al.European journal of human genetics. 2012, Vol 20, Num 5, pp 521-526, issn 1018-4813, 6 p.Article
Autism, language and communication in children with sex chromosome trisomiesBISHOP, Dorothy V. M; JACOBS, Patricia A; SHEARS, Deborah et al.Archives of disease in childhood. 2011, Vol 96, Num 10, pp 954-959, issn 0003-9888, 6 p.Article