2024-03-29T07:12:37Z
http://repoint.unil.ch/oaiprovider/
oai:serval.unil.ch:BIB_0141A423D0A6
2024-03-23T01:47:29Z
serval:BIB_0141A423D0A6
An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient.
10.1038/ejhg.2009.108
000272609900009
19568270
Ferrero
G.B.
author
Howald
C.
author
Micale
L.
author
Biamino
E.
author
Augello
B.
author
Fusco
C.
author
Turturo
M.G.
author
Forzano
S.
author
Reymond
A.
author
Merla
G.
author
article
2010
European Journal of Human Genetics
1476-5438[electronic], 1018-4813[linking]
journal
18
1
33-38
Adult
Child
Chromosome Deletion
Cognition
Female
Genome, Human/genetics
Humans
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Intelligence Tests
Male
Phenotype
Polymerase Chain Reaction
Pregnancy
Williams Syndrome/genetics
eng
60_published
true
peer-reviewed