De Novo and Biallelic Deaf1 Variants Cause a Phenotypic Spectrum

AuthID
P-015-D98
38
Author(s)
Jensik, PJ
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McGee, SR
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Parker, MJ
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Lahiri, N
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McNeil, EP
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Kroes, HY
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Hagerman, RJ
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Harrison, RE
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Montgomery, T
·
[+18]·
Maroofian, R
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Manzini, MC
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Cauley, ES
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Colombo, R
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Odent, S
·
Dubourg, C
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Phornphutkul, C
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de Brouwer, AP
·
de Vries, BB
·
Vulto-vanSilfhout, AT
Document Type
Article
Year published
2019
Published
in Genetics in Medicine, ISSN: 1098-3600
Volume: 21, Issue: 9, Pages: 2059-2069
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Source Identifiers
ISSN: 1098-3600
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Name Order Name   Name Order Name   Name Order Name
1 Nabais Sá, MJ;   2 Jensik, PJ;   3 McGee, SR;
4 Parker, MJ;   5 Lahiri, N;   6 McNeil, EP;
7 Kroes, HY;   8 Hagerman, RJ;   9 Harrison, RE;
10 Montgomery, T;   11 Splitt, M;   12 Palmer, EE;
13 Sachdev, RK;   14 Mefford, HC;   15 Scott, AA;
16 Martinez-Agosto, JA;   17 Lorenz, R;   18 Orenstein, N;
19 Berg, JN;   20 Amiel, J;   21 Heron, D;
22 Keren, B;   23 Cobben, J;   24 Menke, LA;
25 Marco, EJ;   26 Graham, JM;   27 Pierson, TM;
28 Karimiani, EG;   29 Maroofian, R;   30 Manzini, MC;
31 Cauley, ES;   32 Colombo, R;   33 Odent, S;
34 Dubourg, C;   35 Phornphutkul, C;   36 de Brouwer, AP;
37 de Vries, BB;   38 Vulto-vanSilfhout, AT;