Females with de novo aberrations inPHF6: Clinical overlap of Borjeson-Forssman-Lehmann with Coffin-Siris syndrome-Reference-Cited by-同舟云学术

Females with de novo aberrations inPHF6: Clinical overlap of Borjeson-Forssman-Lehmann with Coffin-Siris syndrome

Published:2014-08-05 Issue:3 Volume:166 Page:290-301
ISSN:1552-4868
Container-title:American Journal of Medical Genetics Part C: Seminars in Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Zweier Christiane,Rittinger Olaf,Bader Ingrid,Berland Siren,Cole Trevor,Degenhardt Franziska,Di Donato Nataliya,Graul-Neumann Luitgard,Hoyer Juliane,Lynch Sally Ann,Vlasak Ingrid,Wieczorek Dagmar

Funder

German Ministry of Education and Research BMBF

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference23 articles.

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2. PHF6 deletions may cause Borjeson-Forssman-Lehmann syndrome in females;Berland;Mol Syndromol,2011

3. An X-linked, recessively inherited syndrome characterized by grave mental deficiency, epilepsy, and endocrine disorder;Borjeson;Acta Med Scand,1962

4. The genetic basis of DOORS syndrome: An exome-sequencing study;Campeau;Lancet Neurol,2014

5. The biology of chromatin remodeling complexes;Clapier;Annu Rev Biochem,2009

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