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Molecular Genetics & Genomic Medicine|April 30, 2020
Structural analysis of pathogenic missense mutations in GABRA2 and identification of a novel de novo variant in the desensitization gateAlba Sanchis-Juan, Marcia A Hasenahuer, James A Baker, et al.Molecular Genetics & Genomic Medicine|April 11, 2020
Early behavioral and developmental interventions in ADNP-syndrome: A case report of SWI/SNF-related neurodevelopmental syndromeAmelle Shillington, Ernest Pedapati, Robert Hopkin, et al.Molecular Genetics & Genomic Medicine|July 18, 2018
Frequency of HLA-DQ, susceptibility genotypes for celiac disease, in Brazilian newbornsFernanda C Almeida, Lenora Gandolfi, Karina N Costa, et al.Molecular Genetics & Genomic Medicine|April 7, 2018
A genetic variant in IL-15Rα correlates with physical activity among European-American adultsMichael Bruneau, Sean Walsh, Eric Selinsky, et al.Molecular Genetics & Genomic Medicine|July 14, 2018
Incomplete methylation of a germ cell tumor (Seminoma) in a Prader-Willi maleTalia Eldar-Geva, Varda Gross-Tsur, Harry J Hirsch, et al.Molecular Genetics & Genomic Medicine|July 3, 2018
Establishment of the Alabama Hereditary Cancer Cohort - strategies for the inclusion of underrepresented populations in cancer genetics researchMadison R Bishop, Amit Shah, Melissa Shively, et al.Molecular Genetics & Genomic Medicine|September 22, 2016
Founder mutation in KCNJ10 in Pakistani patients with EAST syndromeOla Abdelhadi, Daniela Iancu, Mehmet Tekman, et al.Molecular Genetics & Genomic Medicine|September 22, 2016
ADGRL3 (LPHN3) variants are associated with a refined phenotype of ADHD in the MTA studyMaria T Acosta, James Swanson, Annamarie Stehli, et al.Molecular Genetics & Genomic Medicine|May 27, 2017
Genetics and genomic medicine in CubaHilda Roblejo Balbuena, Beatriz Marcheco TeruelPageof 251