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Case Reports in Genetics|December 15, 2015
The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati SyndromeMolly B Sheridan, Elizabeth Wohler, Denise A S Batista, et al.Pediatric Pulmonology|July 22, 2025
PulmZoom: Yield for Targeted Gene Panels in Genetically-Mediated Respiratory DisordersSara C Sadreameli, Molly B Sheridan, Sumathi I Rachamadugu, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 15, 2014
The impact of chromosomal microarray on clinical management: a retrospective analysisLindsay B Henderson, Carolyn D Applegate, Elizabeth Wohler, et al.Human Molecular Genetics|October 7, 2005
Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndromeMolly B Sheridan, Peying Fong, Joshua D Groman, et al.JCI Insight|November 14, 2024
Recurrent small variants in NESP55/NESPAS associated with broad GNAS methylation defects and pseudohypoparathyroidism type 1BDong Li, Suzanne Jan de Beur, Cuiping Hou, et al.Journal of Medical Genetics|November 25, 2010
CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTRMolly B Sheridan, Timothy W Hefferon, Nulang Wang, et al.Cancer Genetics|May 13, 2014
Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocationTakema Kato, Colleen P Franconi, Molly B Sheridan, et al.International Journal of Pediatric Otorhinolaryngology|November 6, 2012
A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patientsJosine C C Widdershoven, Mark Bowser, Molly B Sheridan, et al.American Journal of Human Genetics|May 29, 2018
Functional Assays Are Essential for Interpretation of Missense Variants Associated with Variable ExpressivityKaren S Raraigh, Sangwoo T Han, Emily Davis, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Accurate assignment of disease liability to genetic variants using only population dataJoseph M Collaco, Karen S Raraigh, Joshua Betz, et al.Pageof 2