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American Journal of Human Genetics|February 1, 1987
Analysis of fetal intestinal enzymes in amniotic fluid for the prenatal diagnosis of cystic fibrosisR A Mulivor, D Cook, F Muller, et al.American Journal of Human Genetics|April 1, 1987
An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13L A Farrer, P J Goodfellow, C M Lamarche, et al.American Journal of Human Genetics|May 1, 1987
Nonrandom loss of maternal chromosome 11 alleles in Wilms tumorsW T Schroeder, L Y Chao, D D Dao, et al.American Journal of Human Genetics|July 9, 2016
Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with AnemiaNikhita Ajit Bolar, Christelle Golzio, Martina Živná, et al.American Journal of Human Genetics|August 29, 2017
A Scalable Bayesian Method for Integrating Functional Information in Genome-wide Association StudiesJingjing Yang, Lars G Fritsche, Xiang Zhou, et al.American Journal of Human Genetics|June 1, 1987
The coding sequence for the 32,000-dalton pulmonary surfactant-associated protein A is located on chromosome 10 and identifies two separate restriction-fragment-length polymorphismsJ H Fisher, F T Kao, C Jones, et al.American Journal of Human Genetics|September 1, 1986
Genetic analysis of the hypervariable region flanking the human insulin geneP Rotwein, S Yokoyama, D K Didier, et al.American Journal of Human Genetics|August 5, 2017
From Peas to Disease: Modifier Genes, Network Resilience, and the Genetics of HealthJesse D Riordan, Joseph H NadeauAmerican Journal of Human Genetics|August 5, 2017
Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh SyndromeNicole J Lake, Bryn D Webb, David A Stroud, et al.American Journal of Human Genetics|June 14, 2016
Imputing Phenotypes for Genome-wide Association StudiesFarhad Hormozdiari, Eun Yong Kang, Michael Bilow, et al.Pageof 980