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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 10, 2023. (Total: 217827Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Down Syndrome and DYRK1A[original query]
DYRK1A mutations in two unrelated patients.
European journal of medical genetics 2015 Mar 58 (3): 168-74.
Ruaud Lyse, Mignot Cyril, Guët Agnès, Ohl Christelle, Nava Caroline, Héron Delphine, Keren Boris, Depienne Christel, Benoit Valérie, Maystadt Isabelle, Lederer Damien, Amsallem Daniel, Piard Juliet
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID.
Molecular psychiatry 2015 Feb .
van Bon B W M, Coe B P, Bernier R, Green C, Gerdts J, Witherspoon K, Kleefstra T, Willemsen M H, Kumar R, Bosco P, Fichera M, Li D, Amaral D, Cristofoli F, Peeters H, Haan E, Romano C, Mefford H C, Scheffer I, Gecz J, de Vries B B A, Eichler E
Association of the Single Nucleotide Polymorphisms in RUNX1, DYRK1A, and KCNJ15 with Blood Related Traits in Pigs.
Asian-Australasian journal of animal sciences 2016 Dec 29 (12): 1675-1681.
Lee Jae-Bong, Yoo Chae-Kyoung, Park Hee-Bok, Cho In-Cheol, Lim Hyun-T
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