Showing results (1-10 of 83) with videos related to
Sort By:
Pageof 9
American Journal of Medical Genetics. Part A|March 22, 2025
Obesity Prevalence in DDX3X-Related Neurodevelopmental DisorderGiavanna Verdi, Nathaniel H RobinClinical Case Reports|June 12, 2026
Understanding the Role of Genetic Testing in Diagnosing a Complex Pediatric CaseGiavanna Verdi, Aleksandra Foksinska, Elizabeth L Nichols, et al.American Journal of Medical Genetics. Part A|July 2, 2013
Craniosynostosis and radial ray defect: a rare presentation of 22q11.2 deletion syndromeKitiwan Rojnueangnit, Nathaniel H RobinCurrent Opinion in Pediatrics|September 19, 2024
Riding the gene therapy wave: challenges and opportunities for rare disease patients and cliniciansMatthew S Alexander, Nathaniel H RobinClinics in Perinatology|June 5, 2015
Newborn craniofacial malformations: orofacial clefting and craniosynostosisJ Austin Hamm, Nathaniel H RobinPrimary Care|August 28, 2004
The primary care physician's approach to congenital anomaliesMarni J Falk, Nathaniel H RobinJournal of Personalized Medicine|March 21, 2020
Dysmorphology in the Era of Genomic DiagnosisAnna C E Hurst, Nathaniel H RobinJournal of Communication Disorders|August 6, 2002
Genetic testing for deafness--GJB2 and SLC26A4 as causes of deafnessRichard J H Smith, Nathaniel H RobinAmerican Journal of Medical Genetics. Part A|April 18, 2018
Novel de novo pathogenic variant in the NR2F2 gene in a boy with congenital heart defect and dysmorphic featuresJariya Upadia, Patrick R Gonzales, Nathaniel H RobinCurrent Opinion in Pediatrics|September 12, 2014
International adoption of children with birth defects: current knowledge and areas for further researchMeagan E Cochran, Katherine R Nelson, Nathaniel H RobinPageof 9