Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: EVC2[original query] |
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Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations. European journal of human genetics : EJHG 2010 Jun 18 (6): 726-32. Ingersoll Roxann G, Hetmanski Jacqueline, Park Ji-Wan, Fallin M Daniele, McIntosh Iain, Wu-Chou Yah-Huei, Chen Philip K, Yeow Vincent, Chong Samuel S, Cheah Felicia, Sull Jae Woong, Jee Sun Ha, Wang Hong, Wu Tao, Murray Tanda, Huang Shangzhi, Ye Xiaoqian, Jabs Ethylin Wang, Redett Richard, Raymond Gerald, Scott Alan F, Beaty Terri |
Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome. Clinical genetics 2017 9 93 (3): 632-639. Niceta M, Margiotti K, Digilio M C, Guida V, Bruselles A, Pizzi S, Ferraris A, Memo L, Laforgia N, Dentici M L, Consoli F, Torrente I, Ruiz-Perez V L, Dallapiccola B, Marino B, De Luca A, Tartaglia |
Ellis-Van Creveld Syndrome: Clinical and Molecular Analysis of 50 Individuals. Journal of medical genetics 2022 8 . Aubert-Mucca Marion, Huber Céline, Baujat Genevieve, Michot Caroline, Zarhrate Mohammed, Bras Marc, Boutaud Lucile, Malan Valérie, Attie-Bitach Tania, , Cormier-Daire Valer |
Whole exome sequencing of 28 families of Danish descent reveals novel candidate genes and pathways in developmental dysplasia of the hip. Molecular genetics and genomics : MGG 2022 12 298 (2): 329-342. Dembic Maja, van Brakel Andersen Lars, Larsen Martin Jakob, Mechlenburg Inger, Søballe Kjeld, Hertz Jens Micha |
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