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American Journal of Medical Genetics. Part A|March 1, 2005
Carpal and tarsal synostoses and transverse reduction defects of the toes in two brothers heterozygous for a double de novo NOGGIN mutationPhilippe Debeer, Christel Huysmans, Wim J M Van de Ven, et al.Autism : the International Journal of Research and Practice|May 29, 2004
Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autismDries Castermans, Valérie Wilquet, Jean Steyaert, et al.American Journal of Medical Genetics|March 29, 2002
Glypican 1 gene: good candidate for brachydactyly type EMaria Syrrou, Katelÿne Keymolen, Koen Devriendt, et al.Paediatric and Perinatal Epidemiology|January 27, 2005
Gender mix: does it modify birthweight--outcome association?Robert Derom, Catherine Derom, Ruth J F Loos, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 12, 2002
Benign multiple diffuse neonatal hemangiomatosis after a pregnancy complicated by polyhydramnios and a placental chorioangiomaIngrid Witters, Marie Therèse Van Damme, Paul Ramaekers, et al.European Journal of Medical Genetics|July 5, 2008
The genetic basis of inherited anomalies of the teeth. Part 2: syndromes with significant dental involvementIsabelle Bailleul-Forestier, Ariane Berdal, Frans Vinckier, et al.European Journal of Human Genetics : EJHG|January 17, 2003
Psychological distress in the 5-year period after predictive testing for Huntington's diseaseMarleen Decruyenaere, Gerry Evers-Kiebooms, Trees Cloostermans, et al.European Journal of Medical Genetics|August 2, 2005
X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian familyHilde Van Esch, Ginevra Zanni, Maureen Holvoet, et al.Obesity (Silver Spring, Md.)|January 29, 2011
DNA methylation variability at growth-related imprints does not contribute to overweight in monozygotic twins discordant for BMINicole Y P Souren, Sascha Tierling, Jean-Pierre Fryns, et al.Fetal Diagnosis and Therapy|December 15, 2010
Recent developments in the genetic factors underlying congenital diaphragmatic herniaPaul D Brady, Kasemsri Srisupundit, Koenraad Devriendt, et al.Pageof 17