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

Authors :
van Bon, Bregje W M
Koolen, David A
Brueton, Louise
McMullan, Dominic
Lichtenbelt, Klaske D
Adès, Lesley C
Peters, Gregory
Gibson, Kate
Moloney, Susan
Novara, Francesca
Pramparo, Tiziano
Bernardina, Bernardo Dalla
Zoccante, Leonardo
Balottin, Umberto
Piazza, Fausta
Pecile, Vanna
Gasparini, Paolo
Guerci, Veronica
Kets, Marleen
Pfundt, Rolph
Source :
European Journal of Human Genetics; Oct2010, Vol. 18 Issue 10, p1171-1171, 1p
Publication Year :
2010

Abstract

A correction to an article on microdeletion syndrome that was published in the previous issue is presented.

Subjects

Subjects :
GENETICS

Details

Language :
English
ISSN :
10184813
Volume :
18
Issue :
10
Database :
Complementary Index
Journal :
European Journal of Human Genetics
Publication Type :
Academic Journal
Accession number :
53881592
Full Text :
https://doi.org/10.1038/ejhg.2010.103