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De Novo and Biallelic Deaf1 Variants Cause a Phenotypic Spectrum
AuthID
P-015-D98
P-015-D98
38
Author(s)
Jensik, PJ
·McGee, SR
·Parker, MJ
·Lahiri, N
·McNeil, EP
·Kroes, HY
·Hagerman, RJ
·Harrison, RE
·Montgomery, T
·[+18]·
Maroofian, R
·Manzini, MC
·Cauley, ES
·Colombo, R
·Odent, S
·Dubourg, C
·Phornphutkul, C
·de Brouwer, AP
·de Vries, BB
·Vulto-vanSilfhout, AT
Tipo de Documento
Article
Year published
2019
Publicado
in Genetics in Medicine, ISSN: 1098-3600
Volume: 21, Número: 9, Páginas: 2059-2069
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ISSN: 1098-3600
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| Name Order | Nome | Name Order | Nome | Name Order | Nome | ||
|---|---|---|---|---|---|---|---|
| 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; |
