Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: MYO1D[original query] |
---|
High density SNP association study of a major autism linkage region on chromosome 17. Human molecular genetics 2007 Mar 16 (6): 704-15. Stone Jennifer L, Merriman Barry, Cantor Rita M, Geschwind Daniel H, Nelson Stanley |
Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns.
American journal of respiratory and critical care medicine 2014 Aug 190 (4): 399-409. Castaldi Peter J, Cho Michael H, San José Estépar Raúl, McDonald Merry-Lynn N, Laird Nan, Beaty Terri H, Washko George, Crapo James D, Silverman Edwin K, |
Familial Lymphoproliferative Malignancies and Tandem Duplication of NF1 Gene. Case reports in oncological medicine 2015 1 2014 685857. Fernandes Gustavo, Souto Mirela, Costa Frederico, Oliveira Edite, Garicochea Bernar |
Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis.
Human molecular genetics 2022 1 31 (13): 2279-2293. Choquet Hélène, Li Weiyu, Yin Jie, Bradley Rachael, Hoffmann Thomas J, Nandakumar Priyanka, , Mostaedi Rouzbeh, Tian Chao, Ahituv Nadav, Jorgenson Er |
- Page last reviewed:Feb 1, 2024
- Page last updated:Mar 25, 2024
- Content source: