Weaver Syndrome and Ezh2 Mutations: Clarifying the Clinical Phenotype

AuthID
P-00J-7A4
33
Author(s)
Murray, A
·
Hanks, S
·
Douglas, J
·
Armstrong, R
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Banka, S
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Bird, LM
·
Clericuzio, CL
·
Cushing, T
·
[+1]·
[+12]·
Strenger, V
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Stuurman, K
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Taylor, C
·
Titheradge, H
·
Van Maldergem, L
·
Temple, IK
·
Cole, T
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Seal, S
·
Rahman, N
Document Type
Article
Year published
2013
Published
in Am. J. Med. Genet. - American Journal of Medical Genetics Part A, ISSN: 1552-4825
Volume: 161, Issue: 12, Pages: 2972-2980
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ISSN: 1552-4825
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Name Order Name   Name Order Name   Name Order Name
1 Tatton-Brown, K;   2 Murray, A;   3 Hanks, S;
4 Douglas, J;   5 Armstrong, R;   6 Banka, S;
7 Bird, LM;   8 Clericuzio, CL;   9 Cormier-Daire, V;
10 Cushing, T;   11 Flinter, F;   12 Jacquemont, M;
13 Joss, S;   14 Kinning, E;   15 Lynch, SA;
16 Magee, A;   17 McConnell, V;   18 Medeira, A;
19 Ozono, K;   20 Patton, M;   21 Rankin, J;
22 Shears, D;   23 Simon, M;   24 Splitt, M;
25 Strenger, V;   26 Stuurman, K;   27 Taylor, C;
28 Titheradge, H;   29 Van Maldergem, L;   30 Temple, IK;
31 Cole, T;   32 Seal, S;   33 Rahman, N;