Showing results (101-110 of 116) with videos related to
Sort By:
Pageof 12
Journal of Applied Research in Intellectual Disabilities : JARID|July 28, 2026
How Do Parents Experience Overnight Respite? Parent-Reported Outcomes in Families of Children With Intellectual and Developmental DisabilitiesSarah S Mire, Erik W Carter, Sara Tomek, et al.Journal of Craniofacial Genetics and Developmental Biology|January 1, 1981
Trisomy 7 mosaicism and manifestations of Goldenhar syndrome with unilateral radial hypoplasiaM E Hodes, S Gleiser, G P DeRosa, et al.American Journal of Medical Genetics|August 1, 1983
Part II. Amyoplasia: twinning in amyoplasia--a specific type of arthrogryposis with an apparent excess of discordantly affected identical twinsJ G Hall, S D Reed, B C McGillivray, et al.American Journal of Medical Genetics|February 1, 1984
Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new casesR S Young, D D Weaver, M K Kukolich, et al.Public Health Nutrition|July 30, 2021
Mitigating childhood food insecurity during COVID-19: a qualitative study of how school districts in California's San Joaquin Valley responded to growing needsAshley H Jowell, Janine S Bruce, Gabriela V Escobar, et al.American Journal of Medical Genetics|April 15, 2000
Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndromeA E Lin, E V Semina, S Daack-Hirsch, et al.Journal of Medical Genetics|August 14, 2008
Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexiaF E Abidi, L Holloway, C A Moore, et al.Lab on a Chip|November 24, 2020
Correction: A system for the high-throughput measurement of the shear modulus distribution of human red blood cellsAmir Saadat, Diego A Huyke, Diego I Oyarzun, et al.Lab on a Chip|July 11, 2020
A system for the high-throughput measurement of the shear modulus distribution of human red blood cellsAmir Saadat, Diego A Huyke, Diego I Oyarzun, et al.American Journal of Medical Genetics|October 6, 1999
Mild autosomal dominant hypophosphatasia: in utero presentation in two familiesC A Moore, C J Curry, P S Henthorn, et al.Pageof 12