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Molecular Genetics and Metabolism|June 6, 2021
Ultrasound findings of finger, wrist and knee joints in Mucopolysaccharidosis Type IJohannes Roth, Michal Inbar-Feigenberg, Julian Raiman, et al.
Public Health Genomics|October 30, 2019
Family History Taking in Pediatric Practice: A Qualitative Interview StudyLaure Tessier, Jamie C Brehaut, Beth K Potter, et al.
Orphanet Journal of Rare Diseases|August 14, 2025
A cost-utility analysis of newborn screening for spinal muscular atrophy in CanadaAlex Pace, Weston Roda, Corrina Poon, et al.
Children (Basel, Switzerland)|August 26, 2023
Parental Preferences for Expanded Newborn Screening: What Are the Limits?Nicole S Y Liang, Abby Watts-Dickens, David Chitayat, et al.
BMJ Open|February 23, 2022
Cross-sectional prospective feasibility study of newborn screening for sickle cell anaemia and congenital hypothyroidism in GuyanaBibi Areefa Alladin, Pheona Mohamed-Rambaran, Vijay Grey, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
Clinical and genetic aspects of trigonocephaly: a study of 25 casesCyrus Azimi, Shelley J Kennedy, David Chitayat, et al.
BMC Pediatrics|February 4, 2016
Prediction of congenital hypothyroidism based on initial screening thyroid-stimulating-hormoneDavid S Saleh, Sarah Lawrence, Michael T Geraghty, et al.
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