De Novo Variants in Spop Cause Two Clinically Distinct Neurodevelopmental Disorders

AuthID
P-015-D9A
23
Author(s)
El Tekle, G
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de Brouwer, AP
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Sawyer, SL
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del Gaudio, D
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Parker, MJ
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Kanani, F
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van den Boogaard, MH
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van Gassen, K
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Van Allen, MI
·
[+3]·
Begtrup, A
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Keller-Ramey, J
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Bernasocchi, T
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van de Wiel, L
·
Gilissen, C
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Venselaar, H
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Pfundt, R
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Vissers, LE
·
Theurillat, JP
·
de Vries, BB
Document Type
Article
Year published
2020
Published
in The American Journal of Human Genetics, ISSN: 0002-9297
Volume: 106, Issue: 3, Pages: 405-411
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Source Identifiers
ISSN: 0002-9297
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Name Order Name   Name Order Name   Name Order Name
1 Nabais Sá, MJ;   2 El Tekle, G;   3 de Brouwer, AP;
4 Sawyer, SL;   5 del Gaudio, D;   6 Parker, MJ;
7 Kanani, F;   8 van den Boogaard, MH;   9 van Gassen, K;
10 Van Allen, MI;   11 Wierenga, K;   12 Purcarin, G;
13 Elias, ER;   14 Begtrup, A;   15 Keller-Ramey, J;
16 Bernasocchi, T;   17 van de Wiel, L;   18 Gilissen, C;
19 Venselaar, H;   20 Pfundt, R;   21 Vissers, LE;
22 Theurillat, JP;   23 de Vries, BB;