Genome Sequencing and Comprehensive Rare-Variant Analysis of 465 Families with Neurodevelopmental Disorders

AuthID
P-00Y-VMF
31
Author(s)
Sanchis-Juan, A
·
Megy, K
·
Stephens, J
·
Ricaurte, CA
·
Dewhurst, E
·
Low, K
·
French, CE
·
[+3]·
[+1]·
[+7]·
Rankin, J
·
Reid, E
·
Wassmer, E
·
NIHR BioResource
·
Carss, KJ
1
Group Author(s)
Woods, CG
Document Type
Article
Year published
2023
Published
in AMERICAN JOURNAL OF HUMAN GENETICS, ISSN: 0002-9297
Volume: 110, Issue: 8, Pages: 1343-1355 (14)
Indexing
Publication Identifiers
Pubmed: 37541188
SCOPUS: 2-s2.0-85166597588
Wos: WOS:001052932400001
Source Identifiers
ISSN: 0002-9297
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Info
At this moment we don't have any links to full text documens.
Name Order Name   Name Order Name   Name Order Name
1 Sanchis-Juan, A;   2 Megy, K;   3 Stephens, J;
4 Ricaurte, CA;   5 Dewhurst, E;   6 Low, K;
7 French, CE;   8 Grozeva, D;   9 Stirrups, K;
10 Erwood, M;   11 McTague, A;   12 Penkett, CJ;
13 Shamardina, O;   14 Tuna, S;   15 Daugherty, LC;
16 Gleadall, N;   17 Duarte, ST;   18 Hedrera-Fernandez, A;
19 Vogt, J;   20 Ambegaonkar, G;   21 Chitre, M;
22 Josifova, D;   23 Kurian, MA;   24 Parker, A;
25 Rankin, J;   26 Reid, E;   27 Wakeling, E;
28 Wassmer, E;   29 NIHR BioResource;   30 Raymond, FL;
31 Carss, KJ;