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Journal of Attention Disorders|April 24, 2026
ADHD Symptoms, Internalizing Symptoms, and Friendship Features in Emerging Adults: The Moderating Effect of Cognitive Disengagement Syndrome SymptomsNicole F Greenberg, Stephen P Becker, Aaron M Luebbe, et al.American Journal of Diseases of Children (1960)|February 1, 1988
X-linked infantile spinal muscular atrophyF Greenberg, K R Fenolio, J F Hejtmancik, et al.American Journal of Human Genetics|May 1, 1996
Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patientsR C Juyal, L E Figuera, X Hauge, et al.Neurology|September 1, 1991
9p monosomy in a patient with Gilles de la Tourette's syndromeL D Taylor, D B Krizman, J Jankovic, et al.American Journal of Human Genetics|December 1, 1995
Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndromeS H Elsea, R C Juyal, S Jiralerspong, et al.Human Molecular Genetics|April 1, 1995
The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patientsZ Zhao, C C Lee, S Jiralerspong, et al.Journal of Nanobiotechnology|July 2, 2025
Nanomaterial isolated extracellular vesicles enable high precision identification of tumor biomarkers for pancreatic cancer liquid biopsyZachary F Greenberg, Samantha Ali, Andrew Brock, et al.American Journal of Medical Genetics|August 1, 1986
Association of amyoplasia with gastroschisis, bowel atresia, and defects of the muscular layer of the trunkC O Reid, J G Hall, C Anderson, et al.Human Molecular Genetics|September 1, 1992
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysisA Kuwano, A Mutirangura, B Dittrich, et al.Clinical Genetics|November 22, 2011
Towards an evidence-based process for the clinical interpretation of copy number variationE R Riggs, D M Church, K Hanson, et al.Pageof 33