Refinement of the critical 2p25.3 deletion region: The role of MYT1L in intellectual disability and obesity

Genetics in Medicine

Volumn 17, Issue 6, 2015, Pages 460-466

  De Rocker, Nina ^a   Vergult, Sarah ^a   Koolen, David ^b   Jacobs, Eva ^a   Hoischen, Alexander ^b   Zeesman, Susan ^c   Bang, Birgitte ^d   Béna, Frédérique ^e   Bockaert, Nele ^a   Bongers, Ernie M ^b   De Ravel, Thomy ^f   Devriendt, Koenraad ^f   Giglio, Sabrina ^g   Faivre, Laurence ^h   Joss, Shelagh ⁱ   Maas, Saskia ^j   Marle, Nathalie ^h   Novara, Francesca ^k   Nowaczyk, Malgorzata J M ^l   Peeters, Hilde ^f   Polstra, Abeltje ^j   Roelens, Filip ^m   Rosenberg, Carla ⁿ   Thevenon, Julien ^h   Tümer, Zeynep ^o   Vanhauwaert, Suzanne ^a   Varvagiannis, Konstantinos ^e   Willaert, Andy ^a   Willemsen, Marjolein ^b   Willems, Marjolaine ^p   Zuffardi, Orsetta ^k   Coucke, Paul ^a   Speleman, Frank ^a   Eichler, Evan E ^q   Kleefstra, Tjitske ^b   Menten, Björn ^a   more..

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c MCMASTER UNIVERSITY   (Canada)

^d Mental Health Services CPH   (Denmark)

^e GENEVA UNIVERSITY HOSPITALS   (Switzerland)

^f UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^g UNIVERSITY OF FLORENCE   (Italy)

^h Medical University of Dijon   (France)

ⁱ SOUTHERN GENERAL HOSPITAL   (United Kingdom)

^j ACADEMIC MEDICAL CENTER   (Netherlands)

^k UNIVERSITY OF PAVIA   (Italy)

^l MCMASTER UNIVERSITY   (Canada)

^m Heilig Hart Ziekenhuis   (Belgium)

ⁿ UNIVERSITY OF SÃO PAULO   (Brazil)

^o UNIVERSITY OF COPENHAGEN   (Denmark)

^p HÔPITAL ARNAUD DE VILLENEUVE   (France)

^q UNIVERSITY OF WASHINGTON   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN TRANSCRIPTION FACTOR 1L; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; MYT1L PROTEIN, HUMAN; NERVE PROTEIN;

ANIMAL TISSUE; ARTICLE; CHILD; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME DELETION 2P25.3; CHROMOSOME DUPLICATION; CLINICAL ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; FATHER; HUMAN; HUMAN TISSUE; IN SITU HYBRIDIZATION; INTELLECTUAL IMPAIRMENT; MALE; NONHUMAN; OBESITY; POINT MUTATION; POLYMERASE CHAIN REACTION; PROTEIN EXPRESSION; QUANTITATIVE ANALYSIS; ZEBRA FISH; ADOLESCENT; ADULT; ANIMAL; CHROMOSOMAL MAPPING; CHROMOSOME 2; FACIES; FEMALE; GENE DUPLICATION; GENE EXPRESSION; GENETIC ASSOCIATION STUDY; GENETICS; MIDDLE AGED; PRESCHOOL CHILD; YOUNG ADULT;

DANIO RERIO;

ADOLESCENT; ADULT; ANIMALS; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 2; COHORT STUDIES; FACIES; FEMALE; GENE DUPLICATION; GENE EXPRESSION; GENETIC ASSOCIATION STUDIES; HUMANS; INTELLECTUAL DISABILITY; MALE; MIDDLE AGED; NERVE TISSUE PROTEINS; OBESITY; POINT MUTATION; TRANSCRIPTION FACTORS; YOUNG ADULT; ZEBRAFISH;

EID: 84930365191     PISSN: 10983600     EISSN: 15300366     Source Type: Journal    
DOI: 10.1038/gim.2014.124     Document Type: Article

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