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American Journal of Medical Genetics. Part A|November 15, 2007
Acrofacial dysostosis syndrome type Rodriguez: prenatal diagnosis and autopsy findingsDavid Sermer, Nada Quercia, Karen Chong, et al.
The Application of Clinical Genetics|October 17, 2017
Primary ciliary dyskinesia: mechanisms and managementNadirah Damseh, Nada Quercia, Nisreen Rumman, et al.
Journal of Genetic Counseling|June 9, 2016
Risk for Patient Harm in Canadian Genetic Counseling Practice: It's Time to Consider RegulationAndrea L Shugar, Nada Quercia, Christopher Trevors, et al.
BMJ Case Reports|June 21, 2011
Complete deletion of the aprataxin gene: ataxia with oculomotor apraxia type 1 with severe phenotype and cognitive deficitGrace Yoon, Robyn Westmacott, Lynn Macmillan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 16, 2006
Immunohistochemical evaluation of conjunctival fibrillin-1 in Marfan syndromeAnuradha Ganesh, Charles Smith, Wilson Chan, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|February 26, 2025
The Importance of Newborn Genetic Screening for Early Identification of GJB2 and SLC26A4 Related Hearing LossEmily R Wener, Sharon L Cushing, Blake C Papsin, et al.
The Laryngoscope|March 1, 2024
Variants in Genes Associated with Hearing Loss in Children: Prevalence in a Large Canadian CohortEmily R Wener, Jacob D McLennan, Blake C Papsin, et al.
American Journal of Medical Genetics|February 13, 2002
Detecting rearrangements in children using subtelomeric FISH and SKYBlaise Clarkson, Katerina Pavenski, Lucie Dupuis, et al.
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