Showing results (321-330 of 442) with videos related to
Sort By:
Pageof 45
HGG Advances|November 27, 2024
MGA-related syndrome: A proposed novel disorderBobbi McGivern, Michelle M Morrow, Erin Torti, et al.European Journal of Human Genetics : EJHG|January 10, 2026
Experiencing acute genomic care: perspectives from parents in the neonatal and paediatric intensive care units towards rapid genomic sequencingMichael P Mackley, Megan A Dickson, Anna Szuto, et al.Human Mutation|May 3, 2013
PhenoTips: patient phenotyping software for clinical and research useMarta Girdea, Sergiu Dumitriu, Marc Fiume, et al.Journal of Women'S Health (2002)|January 30, 2023
Reproductive Safety of Lurasidone and Quetiapine: Update from the National Pregnancy Registry for Psychiatric MedicationsLee S Cohen, Taylor R Church, Marlene P Freeman, et al.American Journal of Medical Genetics. Part A|December 10, 2022
Fetal akinesia deformation sequence syndrome associated with recessive TTN variantsEbba Alkhunaizi, Nicole Martin, Angie C Jelin, et al.Journal of Medical Genetics|September 21, 2021
Clinical application of fetal genome-wide sequencing during pregnancy: position statement of the Canadian College of Medical GeneticistsJoanna Lazier, Taila Hartley, Jo-Ann Brock, et al.American Journal of Medical Genetics. Part A|May 29, 2012
Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndromeElaine Suk-Ying Goh, Irene C Perez, Cesar P Canales, et al.The Journal of Clinical Psychiatry|October 5, 2021
Correction. Reproductive Safety of Second-Generation Antipsychotics: Updated Data From the Massachusetts General Hospital National Pregnancy Registry for Atypical AntipsychoticsAdele C Viguera, Marlene P Freeman, Lina Góez-Mogollón, et al.American Journal of Medical Genetics. Part A|May 15, 2012
Extracellular matrix and platelet function in patients with musculocontractural Ehlers-Danlos syndrome caused by mutations in the CHST14 geneRoberto Mendoza-Londono, David Chitayat, Walter H A Kahr, et al.American Journal of Medical Genetics. Part A|May 17, 2007
The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): report of eight cases including a living child and further evidence for autosomal recessive inheritanceDavid Chitayat, Hana Sroka, Sarah Keating, et al.Pageof 45