Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD-Reference-Cited by-同舟云学术

Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD

Published:2007-07 Issue:4 Volume:50 Page:301-308
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Lonardo Fortunato,Parenti Giancarlo,Luquetti Daniela Varela,Annunziata Ida,Della Monica Matteo,Perone Lucia,De Gregori Manuela,Zuffardi Orsetta,Brunetti-Pierri Nicola,Andria Generoso,Scarano Gioacchino

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference16 articles.

1. Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome;Ballabio;Proc. Natl. Acad. Sci. USA,1989

2. Association of ADHD and conduct disorder – brain electrical evidence for the existence of a distinct subtype;Banaschewski;J. Child Psychol. Psychiatry,2003

3. Color Atlas of Congenital Malformation Syndromes;Baraitser,1996

4. A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD;Boycott;Am. J. Med. Genet.,2003

5. An Xp; Yq translocation causing a novel contiguous gene syndrome in brothers with generalized epilepsy, ichthyosis, and attention deficits;Doherty;Epilepsia,2003

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