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Hoa Thi Phuong Bui ; Duong Huy Do ; Ha Thi Thanh Ly...
https://figshare.com/articles/journal_contribution/S1_File_-/25362869. , 2024

Link: https://doi.org/10.1371/journal.pone.0290936.s001

RT Journal
T1 <Title>S1 File -</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonianinsp:oai:figshare.com:article_25362869&Exemplar=1&LAN=DE
				
A1 Hoa Thi Phuong Bui
A1 Duong Huy Do
A1 Ha Thi Thanh Ly
A1 Kien Trung Tran
A1 Huong Thi Thanh Le
A1 Kien Trung Nguyen
A1 Linh Thi Dieu Pham
A1 Hau Duc Le
A1 Vinh Sy Le
A1 Arijit Mukhopadhyay
A1 Liem Thanh Nguyen
YR 2024
K1 Genetics
K1 Science Policy
K1 Mental Health
K1 Biological Sciences not elsewhere classified
K1 wide dna microarray
K1 personal development )
K1 fragile x syndrome
K1 exclude rett syndrome
K1 div >< p
K1 detected 1708 non
K1 copy number variations
K1 cnv based test
K1 currently around 10
K1 around 6 %
K1 performed genetic screening
K1 first tier screening
K1 de novo </
K1 autism spectrum disorder
K1 candidate genomic regions
K1 five loss cnvs
K1 3 females )
K1 identified six cnvs
K1 vietnamese asd patients
K1 around 1
K1 six patients
K1 shank3 </
K1 performed genome
K1 developmental disorder
K1 candidate cnvs
K1 candidate genes
K1 redundant cnvs
K1 known cnvs
K1 social interaction
K1 previous reports
K1 patient behaviour
K1 one gain
K1 highest compared
K1 gene –
K1 first report
K1 diagnostic success
K1 deletion involving
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K1 children worldwide
K1 caucasian background
K1 asd patients
K1 7 %)
K1 3 males
K1 100 patients
JF https://figshare.com/articles/journal_contribution/S1_File_-/25362869
LK http://dx.doi.org/https://doi.org/10.1371/journal.pone.0290936.s001
DO https://doi.org/10.1371/journal.pone.0290936.s001
SF ELIB - SuUB Bremen

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