Early-onset obesity and paternal 2pter deletion encompassing the ACP1, TMEM18, and MYT1L genes

European Journal of Human Genetics

Volumn 22, Issue 4, 2014, Pages 471-479

  Doco Fenzy, Martine ^a   Leroy, Camille ^a   Schneider, Anouck ^b   Petit, Florence ^c   Delrue, Marie Ange ^d   Andrieux, Joris ^c   Perrin Sabourin, Laurence ^e   Landais, Emilie ^a   Aboura, Azzedine ^e   Puechberty, Jacques ^b,f   Girard, Manon ^f   Tournaire, Magali ^f   Sanchez, Elodie ^b   Rooryck, Caroline ^d   Ameil, Agnès ^g   Goossens, Michel ^h   Jonveaux, Philippe ⁱ   Lefort, Geneviève ^b,f   Taine, Laurence ^d   Cailley, Dorothée ^d   Gaillard, Dominique ^a   Leheup, Bruno ^j   Sarda, Pierre ^b   Geneviève, David ^b   more..

^a HÔPITAL MAISON BLANCHE   (France)

^b UNIV MONTPELLIER   (France)

^c LILLE UNIVERSITY HOSPITAL   (France)

^d Laboratoire Maladies Rares Génétique et Métabolisme Bordeaux University   (France)

^e HÔPITAL ROBERT DEBRÉ   (France)

^f MONTPELLIER UNIVERSITY HOSPITAL   (France)

^g AMERICAN MEMORIAL HOSPITAL   (France)

^h HENRI MONDOR HOSPITAL   (France)

ⁱ UNIVERSITÉ DE LORRAINE   (France)

^j UNIVERSITY HOSPITAL OF NANCY   (France)

more..

Author keywords

Abnormal behaviour; Deletion 2p25.3; MYT1L; Obesity; TMEM18

Indexed keywords

ACP1 GENE; ARTICLE; BEHAVIOR DISORDER; CHILD; CHROMOSOME 2P; CHROMOSOME ARM; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE DELETION; HETEROZYGOSITY LOSS; HUMAN; HYPERPHAGIA; INTELLECTUAL IMPAIRMENT; MALE; MICROARRAY ANALYSIS; MYT1L GENE; OBESITY; ONSET AGE; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; PXDN GENE; SH3HYL1 GENE; SINGLE NUCLEOTIDE POLYMORPHISM; SNTG2 GENE; TMEM18 GENE; TPO GENE;

CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 2; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MEMBRANE PROTEINS; NERVE TISSUE PROTEINS; OBESITY; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PRADER-WILLI SYNDROME; PROTEIN TYROSINE PHOSPHATASES; PROTO-ONCOGENE PROTEINS; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION; TRANSCRIPTION FACTORS;

EID: 84896543472     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2013.189     Document Type: Article

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