A 3.2Mb Deletion on 18Q12 in a Patient with Childhood Autism and High-Grade Myopia

AuthID
 P-004-13B
19
Author(s)
Lauritsen, MB
·
Moller, M
·
Henriksen, KF
·
Cintin, C
·
Andersen, PS
·
Rosenberg, T
·
Brondum Nielsen, K
·
Cotterill, RMJ
·
Ropers, HH
·
Ullmann, R
·
Tipo de Documento
Article
Year published
2008
Publicado
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 16, Número: 3, Páginas: 312-319 (8)
Indexing
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Scopus®
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Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 18183041
SCOPUS: 2-s2.0-39749161050
Wos: WOS:000253406900006
Source Identifiers
ISSN: 1018-4813
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