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Military Medicine|January 29, 2020
Effects of Brief Depression and Anxiety Management Training on a US Army Division's Primary Care ProvidersRohul Amin, Mary Ann ThomasAmerican Journal of Medical Genetics. Part A|June 19, 2025
A Population-Based Study of Limb Body Wall Complex With Proposed Features for Prenatal DiagnosisMary Ann Thomas, Susan Crawford, Tanya BedardJournal of Cutaneous Medicine and Surgery|May 16, 2013
Ulerythema ophryogenes, a rarely reported cutaneous manifestation of noonan syndrome: case report and review of the literatureKayi Li, Mary Ann Thomas, Richard M HaberPsychiatric Genetics|November 29, 2023
Maternal 15q11.2-q13.1 duplication syndrome-associated psychosis and mania: a new case and review of the literatureMark Ainsley Colijn, Christopher S Smith, Mary Ann ThomasFetal and Pediatric Pathology|January 11, 2023
Prenatal Diagnosis of Isolated Right Ventricular Non-Compaction Cardiomyopathy with an <i>MYH7</i> Likely Pathogenic VariantWeiming Yu, Mary Ann Thomas, Lindsay Mills, et al.The Journal of Otolaryngology|April 22, 2005
Connexin mutation testing of children with nonsyndromic, autosomal recessive sensorineural hearing lossMary Ann Thomas, Vazken M Der Kaloustian, Ted L TewfikJournal of Pediatric Hematology/Oncology|November 9, 2020
Diffuse Intracerebral Hemorrhage in an Infant With a Novel Homozygous Variant Leading to Severe Protein C DeficiencyGeorgina Martin, Mary Ann Thomas, Xing-Chang Wei, et al.American Journal of Medical Genetics. Part A|March 30, 2024
Prenatal findings in 11 cases with craniofacial microsomia using the Alberta Congenital Anomalies Surveillance System, 1997-2019Mary Ann Thomas, Tanya Bedard, Susan Crawford, et al.American Journal of Medical Genetics. Part A|August 20, 2016
Review of the recurrent 8q13.2q13.3 branchio-oto-renal related microdeletion, and report of an additional case with associated distal arthrogryposisPing-Yee Billie Au, Judy E Chernos, Mary Ann ThomasGenetics in Medicine : Official Journal of the American College of Medical Genetics|March 11, 2020
Re-evaluating the first-tier status of fragile X testing in neurodevelopmental disordersLauren A Borch, Jillian Parboosingh, Mary Ann Thomas, et al.Pageof 5