Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Intellectual Disability and ZMYND11[original query] |
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Refining analyses of copy number variation identifies specific genes associated with developmental delay. Nature genetics 2014 Oct 46 (10): 1063-71. Coe Bradley P, Witherspoon Kali, Rosenfeld Jill A, van Bon Bregje W M, Vulto-van Silfhout Anneke T, Bosco Paolo, Friend Kathryn L, Baker Carl, Buono Serafino, Vissers Lisenka E L M, Schuurs-Hoeijmakers Janneke H, Hoischen Alex, Pfundt Rolph, Krumm Nik, Carvill Gemma L, Li Deana, Amaral David, Brown Natasha, Lockhart Paul J, Scheffer Ingrid E, Alberti Antonino, Shaw Marie, Pettinato Rosa, Tervo Raymond, de Leeuw Nicole, Reijnders Margot R F, Torchia Beth S, Peeters Hilde, O'Roak Brian J, Fichera Marco, Hehir-Kwa Jayne Y, Shendure Jay, Mefford Heather C, Haan Eric, Gécz Jozef, de Vries Bert B A, Romano Corrado, Eichler Evan |
Assessment of Potential Clinical Role for Exome Sequencing in Schizophrenia. Schizophrenia bulletin 2019 5 46 (2): 328-335. Balakrishna Thivia, Curtis Dav |
Intragenic Deletion of the ZMYND11 Gene in 10p15.3 is Associated with Developmental Delay Phenotype: A Case Report. Cytogenetic and genome research 2021 11 161 (8-9): 445-448. Huynh Minh-Tuan, Tran Cong Toai, Joubert Madeleine, Bénéteau Clai |
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- Page last updated:Apr 29, 2024
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