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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 1, 2023. (Total: 221588Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Intellectual Disability and ZEB2[original query]
Sleep disturbance in Mowat-Wilson syndrome.
American journal of medical genetics. Part A 2015 Dec .
Evans Elizabeth, Mowat David, Wilson Meredith, Einfeld Stewa
Copy Number Variants Associated with 14 Cases of Self-Injurious Behavior.
PloS one 2016 11 (3): e0149646.
Shirley Matthew D, Frelin Laurence, López José Soria, Jedlicka Anne, Dziedzic Amanda, Frank-Crawford Michelle A, Silverman Wayne, Hagopian Louis, Pevsner Jonath
Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus and intellectual disability.
Journal of medical genetics 2020 4 57 (7): 466-474.
Chevarin Martin, Duffourd Yannis, A Barnard Rebecca, Moutton Sébastien, Lecoquierre François, Daoud Fatma, Kuentz Paul, Cabret Caroline, Thevenon Julien, Gautier Elodie, Callier Patrick, St-Onge Judith, Jouan Thibaud, Lacombe Didier, Delrue Marie Ange, Goizet Cyril, Morice-Picard Fanny, Van-Gils Julien, Munnich Arnold, Lyonnet Stanislas, Cormier-Daire Valérie, Baujat Geneviève, Holder Muriel, Petit Florence, Leheup Bruno, Odent Sylvie, Jouk Pierre-Simon, Lopez Gipsy, Geneviève David, Collignon Patrick, Martin-Coignard Dominique, Jacquette Aurélia, Perrin Laurence, Putoux Audrey, Sarrazin Elisabeth, Amarof Khadija, Missotte Isabelle, Coubes Christine, Jagadeesh Sujatha, Lapi Elisabetta, Demurger Florence, Goldenberg Alice, Doco-Fenzy Martine, Mignot Cyril, Héron Delphine, Jean-Marçais Nolwenn, Masurel Alice, El Chehadeh Salima, Marle Nathalie, Huet Frédéric, Binquet Christine, Collod-Beroud Gwenaëlle, Arnaud Pauline, Hanna Nadine, Boileau Catherine, Jondeau Guillaume, Olaso Robert, Lechner Doris, Poe Charlotte, Assoum Mirna, Carmignac Virginie, Duplomb Laurence, Tran Mau-Them Frédéric, Philippe Christophe, Vitobello Antonio, Bruel Ange-Line, Boland Anne, Deleuze Jean-François, Thauvin-Robinet Christel, Rivière Jean-Baptiste, O'Roak Brian J, Faivre Lauren
Genotype-phenotype analysis in Mowat-Wilson syndrome associated with two novel and two recurrent variants.
Experimental and therapeutic medicine 2020 Dec 20 (6): 263.
Zou Dongfang, Wang Lin, Wen Feiqiu, Xiao Hongdou, Duan Jing, Zhang Tongda, Yin Zhenzhen, Dong Qiwen, Guo Jian, Liao Jianxia
Three Novel De Novo ZEB2 Variants Identified in Three Unrelated Chinese Patients With Mowat-Wilson Syndrome and A Systematic Review.
Frontiers in genetics 2022 6 13 853183.
Fu Youqing, Xu Wanfang, Wang Qingming, Lin Yangyang, He Peiqing, Liu Yanhui, Yuan Haimi
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