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Year Number of Results
1959 1
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2011 6
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2015 8
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Similar articles for PMID: 29260337

71 results

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Page 1
Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual Disability.
Heide S, Keren B, Billette de Villemeur T, Chantot-Bastaraud S, Depienne C, Nava C, Mignot C, Jacquette A, Fonteneau E, Lejeune E, Mach C, Marey I, Whalen S, Lacombe D, Naudion S, Rooryck C, Toutain A, Caignec CL, Haye D, Olivier-Faivre L, Masurel-Paulet A, Thauvin-Robinet C, Lesne F, Faudet A, Ville D, des Portes V, Sanlaville D, Siffroi JP, Moutard ML, Héron D. Heide S, et al. J Pediatr. 2017 Jun;185:160-166.e1. doi: 10.1016/j.jpeds.2017.02.023. Epub 2017 Mar 8. J Pediatr. 2017. PMID: 28284480
A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.
Derks EM, Ayub M, Chambert K, Del Favero J, Johnstone M, MacGregor S, Maclean A, McKechanie AG, McRae AF, Moran JL, Pickard BS, Purcell S, Sklar P, StClair DM, Wray NR, Visscher PM, Blackwood DH. Derks EM, et al. Am J Med Genet B Neuropsychiatr Genet. 2013 Dec;162B(8):847-54. doi: 10.1002/ajmg.b.32189. Epub 2013 Sep 25. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 24115684
Gonadal mosaicism of large terminal de novo duplication and deletion in siblings with variable intellectual disability phenotypes.
Rahman MM, Uddin KF, Al Jezawi NK, Karuvantevida N, Akter H, Dity NJ, Rahaman MA, Begum M, Rahaman MA, Baqui MA, Salwa Z, Islam S, Woodbury-Smith M, Basiruzzaman M, Uddin M. Rahman MM, et al. Mol Genet Genomic Med. 2019 Oct;7(10):e00954. doi: 10.1002/mgg3.954. Epub 2019 Sep 1. Mol Genet Genomic Med. 2019. PMID: 31475484 Free PMC article.
The effect of copy number variations in chromosome 16p on body weight in patients with intellectual disability.
Gimeno-Ferrer F, Albuquerque D, Guzmán Luján C, Marcaida Benito G, Torreira Banzas C, Repáraz-Andrade A, Ballesteros Cogollos V, Aleu Pérez-Gramunt M, Galán Gómez E, Quintela I, Rodríguez-López R. Gimeno-Ferrer F, et al. J Hum Genet. 2019 Mar;64(3):221-231. doi: 10.1038/s10038-018-0545-5. Epub 2018 Dec 5. J Hum Genet. 2019. PMID: 30518945
71 results