372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment-Reference-Cited by-同舟云学术

372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment

Published:2012-03 Issue:3 Volume:55 Page:216-221
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Marseglia Giuseppina,Scordo Maria Rosaria,Pescucci Chiara,Nannetti Genni,Biagini Elisabetta,Scandurra Valeria,Gerundino Francesca,Magi Alberto,Benelli Matteo,Torricelli Francesca

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

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4. Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases;Poissonnier;Ann. Genet.,1992

5. Long-term survival in a patient with del(18)(q12.2q21.1);Tinkle;Am. J. Med. Genet.,2003

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