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American Journal of Medical Genetics. Part A|December 21, 2002
Further delineation of the Toriello-Carey syndrome: a report of two siblingsIngeborg Barisic, Branimir Peter, Lili MikecinJournal of Applied Genetics|January 13, 2011
Hypochondroplasia due to FGFR3 gene mutation (N540K) and mosaic form of Down syndrome in the same patientKatja Dumic, Ingeborg Barisic, Kristina Potocki, et al.Journal of Pediatric Urology|November 4, 2008
Congenital hydronephrosis: prenatal diagnosis and epidemiology in EuropeEster Garne, Maria Loane, Diana Wellesley, et al.Molecular Cytogenetics|February 7, 2013
Multiplex ligation-dependent probe amplification workflow for the detection of submicroscopic chromosomal abnormalities in patients with developmental delay/intellectual disabilityLeona Morozin Pohovski, Katja K Dumic, Ljubica Odak, et al.European Journal of Pediatrics|October 18, 2006
Enzyme replacement therapy in two patients with an advanced severe (Hurler) phenotype of mucopolysaccharidosis IVisnja Tokic, Ingeborg Barisic, Nevenka Huzjak, et al.Prenatal Diagnosis|July 19, 2002
Prenatal ultrasonographic detection of gastrointestinal obstruction: results from 18 European congenital anomaly registriesMartin C H Haeusler, Andrea Berghold, Claude Stoll, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|March 9, 2011
Paper 1: The EUROCAT network--organization and processesPatricia A Boyd, Martin Haeusler, Ingeborg Barisic, et al.International Journal of Endocrinology|July 3, 2014
Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian Families with 11 β -Hydroxylase DeficiencyKatja Dumic, Tony Yuen, Zorana Grubic, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 5, 2009
Congenital hydrocephalus--prevalence, prenatal diagnosis and outcome of pregnancy in four European regionsEster Garne, Maria Loane, Marie-Claude Addor, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|March 9, 2011
Paper 5: Surveillance of multiple congenital anomalies: implementation of a computer algorithm in European registers for classification of casesEster Garne, Helen Dolk, Maria Loane, et al.Pageof 7