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Genes|September 23, 2022
TBX3 and EFNA4 Variant in a Family with Ulnar-Mammary Syndrome and Sagittal CraniosynostosisMoon Ley Tung, Bharatendu Chandra, Jaclyn Kotlarek, et al.Journal of Neurosurgery|November 26, 2022
A likely HOXC4 predisposition variant for Chiari malformationsDouglas L Brockmeyer, Samuel H Cheshier, Jeff Stevens, et al.International Journal of Cancer|March 14, 2023
A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall-cell lung cancerLisa A Cannon-Albright, Craig C Teerlink, Jeff Stevens, et al.Genes and Immunity|July 24, 2023
Transmission disequilibrium analysis of whole genome data in childhood-onset systemic lupus erythematosusKathleen M Vazzana, Anthony M Musolf, Joan E Bailey-Wilson, et al.Molecular Vision|February 1, 2018
Myopia in Chinese families shows linkage to 10q26.13Anthony M Musolf, Claire L Simpson, Kyle A Long, et al.Investigative Ophthalmology & Visual Science|July 9, 2021
Myopia in African Americans Is Significantly Linked to Chromosome 7p15.2-14.2Claire L Simpson, Anthony M Musolf, Roberto Y Cordero, et al.Genes|May 28, 2022
Targeted Sequencing of Candidate Regions Associated with Sagittal and Metopic Nonsyndromic CraniosynostosisCristina M Justice, Anthony M Musolf, Araceli Cuellar, et al.Statistical Applications in Genetics and Molecular Biology|March 19, 2013
A novel method for analyzing genetic association with longitudinal phenotypesDouglas Londono, Kuo-mei Chen, Anthony Musolf, et al.BMC Medical Genetics|February 2, 2019
Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish familiesClaire L Simpson, Anthony M Musolf, Qing Li, et al.European Journal of Human Genetics : EJHG|June 23, 2019
Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencingAnthony M Musolf, Winson S C Ho, Kyle A Long, et al.Pageof 8