Showing results (151-160 of 170) with videos related to
Sort By:
Pageof 17
American Journal of Medical Genetics|August 22, 1997
Prenatal detection and molecular characterization of a de novo duplication of the distal long arm of chromosome 19P D Cotter, L D McCurdy, I F Gershin, et al.American Journal of Medical Genetics|October 26, 1999
Familial patent ductus arteriosus and bicuspid aortic valve with hand anomalies: a novel heart-hand syndromeB D Gelb, J Zhang, R J Sommer, et al.Clinical Genetics|March 31, 1998
Mosaicism for a small supernumerary ring X chromosome in a dysmorphic, growth-retarded male: mos47,XXY/48,XXY, +r(X)S R Manea, I F Gershin, A Babu, et al.American Journal of Medical Genetics|April 15, 1994
Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G)G M Pastores, F M Santorelli, S Shanske, et al.Journal of Intellectual Disability Research : JIDR|August 6, 2014
'It's made all of us bond since that course…' - a qualitative study of service users' experiences of a CBT anger management group interventionP MacMahon, B Stenfert Kroese, A Jahoda, et al.American Journal of Human Genetics|June 13, 1998
Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosisB D Gelb, J P Willner, T M Dunn, et al.Brain Research|November 11, 2010
Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilitiesAlexander Kolevzon, Guiqing Cai, Latha Soorya, et al.Journal of Psychopharmacology (Oxford, England)|February 12, 2010
A pharmacological tool to assess vasopressinergic co-activation of the hypothalamus-pituitary-adrenal axis more integrally in healthy volunteersG E Jacobs, J M A van Gerven, M l de Kam, et al.Psychopharmacology|January 1, 1991
Voltammetric evidence that subsensitivity to reward following chronic mild stress is associated with increased release of mesolimbic dopamineJ A Stamford, R Muscat, J J O'Connor, et al.American Journal of Medical Genetics|February 7, 1998
Prenatal diagnosis of a familial interchromosomal insertion of Y chromosome heterochromatinP Ashton-Prolla, I F Gershin, A Babu, et al.Pageof 17