2024-03-28T11:34:51Z
http://repoint.unil.ch/oaiprovider/
oai:serval.unil.ch:BIB_079DC291A483
2024-03-23T01:48:55Z
serval:BIB_079DC291A483
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe.
10.1038/ejhg.2011.246
000303016800017
22234154
Wellesley
D.
author
Dolk
H.
author
Boyd
P.A.
author
Greenlees
R.
author
Haeusler
M.
author
Nelen
V.
author
Garne
E.
author
Khoshnood
B.
author
Doray
B.
author
Rissmann
A.
author
Mullaney
C.
author
Calzolari
E.
author
Bakker
M.
author
Salvador
J.
author
Addor
M.C.
author
Draper
E.
author
Rankin
J.
author
Tucker
D.
author
article
2012
European Journal of Human Genetics : Ejhg
1476-5438
1018-4813
journal
20
5
521-526
Abnormalities, Multiple/epidemiology
Abnormalities, Multiple/genetics
Chromosome Aberrations
Chromosome Disorders/epidemiology
Chromosome Disorders/genetics
Chromosomes, Human, Pair 13/genetics
Chromosomes, Human, Pair 18/genetics
Down Syndrome/epidemiology
Down Syndrome/genetics
Europe/epidemiology
Humans
Prenatal Diagnosis/methods
Prevalence
Registries
Trisomy/genetics
eng
60_published
true
Publication types: Journal Article ; Research Support, Non-U.S. Gov't