✦ LIBER ✦

Clinical phenotype and candidate genes for the 5q31.3 microdeletion syndrome

✍ Scribed by Kana Hosoki; Tohru Ohta; Jun Natsume; Sumiko Imai; Akihisa Okumura; Takeshi Matsui; Naoki Harada; Carlos A. Bacino; Fernando Scaglia; Jeremy Y. Jones; Norio Niikawa; Shinji Saitoh

Book ID: 111995259
Publisher: John Wiley and Sons
Year: 2012
Tongue: English
Weight: 256 KB
Volume: 158A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.35439

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The 2q23.1 microdeletion syndrome: clini

The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

✍ van Bon, Bregje WM; Koolen, David A; Brueton, Louise; McMullan, Dominic; Lichten 📂 Article 📅 2009 🏛 Nature Publishing Group 🌐 English ⚖ 628 KB

The 2q23.1 microdeletion syndrome: clini

The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

✍ van Bon, Bregje W M; Koolen, David A; Brueton, Louise; McMullan, Dominic; Lichte 📂 Article 📅 2010 🏛 Nature Publishing Group 🌐 English ⚖ 61 KB

Phenotypic expansion and further charact

Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome

✍ Tan, T Y; Aftimos, S; Worgan, L; Susman, R; Wilson, M; Ghedia, S; Kirk, E P; Lov 📂 Article 📅 2009 🏛 BMJ Publishing Group 🌐 English ⚖ 620 KB

Corrigendum to: The 2q23.1 microdeletion

Corrigendum to: The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

✍ van Bon, Bregje WM; Koolen, David A; Brueton, Louise; McMullan, Dominic; Lichten 📂 Article 📅 2010 🏛 Nature Publishing Group 🌐 English ⚖ 75 KB

P-700 - Social cognition and the behavio

P-700 - Social cognition and the behavioural phenotype of 17q21.31 microdeletion syndrome

✍ J.I.M. Egger; E. Wingbermühle; W.M.A. Verhoeven; M. Dijkman; R.P.C. Kessels; D. 📂 Article 📅 2012 🏛 Elsevier Science 🌐 French ⚖ 93 KB

Mutation screening of the 3q29 microdele

Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia

✍ L.S. Carroll; H.J. Williams; J. Walters; G. Kirov; M.C. O'Donovan; M.J. Owen 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 109 KB 👁 2 views

## Abstract Deletion of chromosome 3q29, which is associated with mental retardation and autism, was recently identified as being present in excess or occurring de novo in schizophrenia cases, being present in approximately 1/1,000 cases and 1/40,000 unscreened controls. Of the ∼20 genes in the com