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American Journal of Human Genetics|November 3, 2015
Privacy Risks from Genomic Data-Sharing BeaconsSuyash S Shringarpure, Carlos D BustamanteAmerican Journal of Human Genetics|November 3, 2015
Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid CancerLamis Yehia, Farshad Niazi, Ying Ni, et al.American Journal of Human Genetics|February 1, 1989
Prenatal diagnosis of Duchenne muscular dystrophy: prospective linkage analysis and retrospective dystrophin cDNA analysisP A Ward, J F Hejtmancik, J A Witkowski, et al.American Journal of Human Genetics|November 7, 2015
Dominant Genetic Variation and Missing Heritability for Human Complex Traits: Insights from Twin versus Genome-wide Common SNP ModelsXu Chen, Ralf Kuja-Halkola, Iffat Rahman, et al.American Journal of Human Genetics|November 7, 2015
Association between Rare Variants in AP4E1, a Component of Intracellular Trafficking, and Persistent StutteringM Hashim Raza, Rafael Mattera, Robert Morell, et al.American Journal of Human Genetics|October 22, 2013
SCRIB and PUF60 are primary drivers of the multisystemic phenotypes of the 8q24.3 copy-number variantAndrew Dauber, Christelle Golzio, Cécile Guenot, et al.American Journal of Human Genetics|October 22, 2013
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humansJan Halbritter, Albane A Bizet, Miriam Schmidts, et al.American Journal of Human Genetics|September 24, 2013
Genetic mapping with multiple levels of phenotypic information reveals determinants of lymphocyte glucocorticoid sensitivityJoseph C Maranville, Shaneen S Baxter, David B Witonsky, et al.American Journal of Human Genetics|December 24, 2013
Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm developmentMyriam Peyrard-Janvid, Elizabeth J Leslie, Youssef A Kousa, et al.American Journal of Human Genetics|December 24, 2013
A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defectsFrancine P Favaro, Lucas Alvizi, Roseli M Zechi-Ceide, et al.Pageof 979