16q12.2q21: A new susceptibility locus for schizophrenia?

被引：2

作者：

Poisson, A. ^{[1
,2
,3
]}

Schluth-Bolard, C. ^{[4
,5
]}

Martin, B. ^{[6
,7
]}

Babinet, M. N. ^{[1
,2
,3
]}

Sanlaville, D. ^{[4
,5
]}

Demily, C. ^{[1
,2
,3
]}

机构：

[1] Ctr Hosp Vinatier, Ctr Diag & Management Genet Psychiat Disorders, GenoPsy, Lyon, France

[2] CNRS, EDR Psy Team, Lyon, France

[3] Lyon 1 Claude Bernard Univ, Lyon, France

[4] HCL, Dept Genet, Reference Ctr Dev Anomalies & Malformat Syndromes, Bron, France

[5] UCBL1, Ctr Rech Neurosci Lyon, GENDEV, INSERM U1028,CNRS UMR529, Lyon, France

[6] CNRS, SUR CL3R, UMR 5229, Bron, France

[7] Univ Lyon 1, CH Vinatier, Bron, France

来源：

SCHIZOPHRENIA RESEARCH | 2016年 / 178卷 / 1-3期

关键词：

DUPLICATION; 16Q; PATIENT;

D O I：

10.1016/j.schres.2016.09.007

中图分类号：

R749 [精神病学];

学科分类号：

100205 ;

摘要：

引用

页码：109 / 111

页数：3

共 10 条

[1] Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect [J].

Barber, J. C. K. ;

Zhang, S. ;

Friend, N. ;

Collins, A. L. ;

Maloney, V. K. ;

Hastings, R. ;

Farren, B. ;

Barnicoat, A. ;

Polityko, A. D. ;

Rumyantseva, N. V. ;

Starke, H. ;

Ye, S. .

CYTOGENETIC AND GENOME RESEARCH, 2006, 114 (3-4) :351-358

[2]

Engelen JJM, 1999, ANN GENET-PARIS, V42, P101

[3]

FRYNS JP, 1990, ANN GENET-PARIS, V33, P46

[4] Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifida [J].

Gustavsson, Peter ;

Schoumans, Jacqueline ;

Staaf, Johan ;

Borg, Ake ;

Nordenskjold, Magnus ;

Anneren, Goran .

EUROPEAN JOURNAL OF MEDICAL GENETICS, 2007, 50 (03) :237-241

[5] Clinical, Cytogenetic and Molecular-Cytogenetic Characterization of a Patient With a De Novo Tandem Proximal-Intermediate Duplication of 16q and Review of the Literature [J].

Lonardo, Fortunato ;

Perone, Lucia ;

Maioli, Marianna ;

Ciavarella, Maria ;

Ciccone, Roberto ;

Della Monica, Matteo ;

Lombardi, Cinzia ;

Forino, Luisa ;

Cantalupo, Giuseppina ;

Masella, Lucia ;

Scarano, Francesca .

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2011, 155A (04) :769-777

[6] AUTISM, MENTAL-RETARDATION, AND CHROMOSOMAL-ABNORMALITIES [J].

MARINER, R ;

JACKSON, AW ;

LEVITAS, A ;

HAGERMAN, RJ ;

BRADEN, M ;

MCBOGG, PM ;

SMITH, ACM ;

BERRY, R .

JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 1986, 16 (04) :425-440

[7] High rates of schizophrenia in adults with velo-cardio-facial syndrome [J].

Murphy, KC ;

Jones, LA ;

Owen, MJ .

ARCHIVES OF GENERAL PSYCHIATRY, 1999, 56 (10) :940-945

[8] Novel duplication on chromosome 16 (q12.1-q21) associated with behavioral disorder, mild cognitive impairment, speech delay, and dysmorphic features: case report [J].

Odak, Ljubica ;

Barisic, Ingeborg ;

Pohovski, Leona Morozin ;

Riegel, Mariluce ;

Schinzel, Albert .

CROATIAN MEDICAL JOURNAL, 2011, 52 (03) :415-422

[9] DIRECT INTRACHROMOSOMAL DUPLICATION OF 16Q AND HERITABLE FRAGILE SITE FRA (10) (Q25) IN THE SAME PATIENT [J].

ROMAIN, DR ;

FRAZER, AG ;

COLUMBANOGREEN, LM ;

PARFITT, RG ;

SMYTHE, RH ;

CHAPMAN, CJ .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 19 (03) :507-513

[10] Atypical Antipsychotics and Relapsing Psychoses in 22q11.2 Deletion Syndrome: A Long-term Evaluation of 28 Patients [J].

Verhoeven, W. M. A. ;

Egger, J. I. M. .

PHARMACOPSYCHIATRY, 2015, 48 (03) :104-110

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