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American Journal of Human Genetics|June 1, 1986
The use of restriction fragment length polymorphisms in paternity analysisP E Smouse, R ChakrabortyAmerican Journal of Human Genetics|September 28, 2021
High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish populationTadahiro Mitani, Sedat Isikay, Alper Gezdirici, et al.American Journal of Human Genetics|June 11, 2019
Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to AsthenozoospermiaMarjorie Whitfield, Lucie Thomas, Emilie Bequignon, et al.American Journal of Human Genetics|June 11, 2019
Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related DisordersYun Tian, Jun-Ling Wang, Wen Huang, et al.American Journal of Human Genetics|October 1, 1989
Detection of marker associations with a dominant disease gene in genetically complex and heterogeneous diseasesE S Gershon, M Martinez, L Goldin, et al.American Journal of Human Genetics|October 1, 1989
Gene inactivation as a mechanism for the expression of recessive phenotypesS G Grant, C E Campbell, C Duff, et al.American Journal of Human Genetics|January 1, 1989
Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1)B R Seizinger, G E Farmer, J L Haines, et al.American Journal of Human Genetics|January 1, 1989
Linkage analysis of neurofibromatosis type I, using chromosome 17 DNA markersS D Kittur, M M Bagdon, M L Lubs, et al.American Journal of Human Genetics|January 1, 1989
Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17J W Fountain, M R Wallace, A M Brereton, et al.American Journal of Human Genetics|June 24, 2014
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP ConsortiaJeannette Simino, Gang Shi, Joshua C Bis, et al.Pageof 979