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Hans Matsson

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European Journal of Human Genetics : EJHG|January 31, 2018

Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locusJoão Fadista, Marie Lund, Line Skotte, et al.

Scientific Reports|August 26, 2017

Identification of NCAN as a candidate gene for developmental dyslexiaElisabet Einarsdottir, Myriam Peyrard-Janvid, Fahimeh Darki, et al.

Human Molecular Genetics|October 20, 2007

Alpha-cardiac actin mutations produce atrial septal defectsHans Matsson, Jacqueline Eason, Carol S Bookwalter, et al.

American Journal of Human Genetics|April 17, 2025

Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorderStephanie Efthymiou, Cailyn P Leo, Chenghong Deng, et al.

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Search research articles

Showing results (31-40 of 34) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 34 results.

European Journal of Human Genetics : EJHG|January 31, 2018

Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locusJoão Fadista, Marie Lund, Line Skotte, et al.

Scientific Reports|August 26, 2017

Identification of NCAN as a candidate gene for developmental dyslexiaElisabet Einarsdottir, Myriam Peyrard-Janvid, Fahimeh Darki, et al.

Human Molecular Genetics|October 20, 2007

Alpha-cardiac actin mutations produce atrial septal defectsHans Matsson, Jacqueline Eason, Carol S Bookwalter, et al.

American Journal of Human Genetics|April 17, 2025

Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorderStephanie Efthymiou, Cailyn P Leo, Chenghong Deng, et al.

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