Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

C Bacci, R Sestini, A Provenzano, I Paganini, I Mancini… - Neurogenetics, 2010 - Springer
Schwannomatosis (MIM 162091) is a condition predisposing to the development of central
and peripheral schwannomas; most cases are sporadic without a clear family history but a …
被引用次数：103 相关文章

[引用][C] Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

C BACCI, R SESTINI, A PROVENZANO… - Neurogenetics …, 2010 - pascal-francis.inist.fr
Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation
CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple search …

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

C Bacci, R Sestini, A Provenzano, I Paganini… - …, 2010 - search.proquest.com
Schwannomatosis (MIM 162091) is a condition predisposing to the development of central
and peripheral schwannomas; most cases are sporadic without a clear family history but a …

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

C Bacci, R Sestini, A Provenzano… - …, 2010 - pubmed.ncbi.nlm.nih.gov
Schwannomatosis (MIM 162091) is a condition predisposing to the development of central
and peripheral schwannomas; most cases are sporadic without a clear family history but a …

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

C Bacci, R Sestini, A Provenzano, I Paganini… - …, 2010 - flore.unifi.it
Schwannomatosis (MIM 162091) is a condition predisposing to the development of central
and peripheral schwannomas; most cases are sporadic without a clear family history but a …

[引用][C] Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

C Bacci, R Sestini, A Provenzano, I Paganini, I Mancini… - neurogenetics, 2009 - cir.nii.ac.jp

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

C Bacci, R Sestini, A Provenzano, I Paganini… - …, 2010 - publicatt.unicatt.it
Schwannomatosis (MIM 162091) is a condition predisposing to the development of central
and peripheral schwannomas; most cases are sporadic without a clear family history but a …
[PDF] researchgate.net

[PDF][PDF] Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

C Bacci, R Sestini, A Provenzano, I Paganini… - …, 2010 - researchgate.net
Schwannomatosis (MIM 162091) is a condition predisposing to the development of central
and peripheral schwannomas; most cases are sporadic without a clear family history but a …

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

C Bacci, R Sestini, A Provenzano, I Paganini, I Mancini… - neurogenetics, 2010 - infona.pl
Schwannomatosis (MIM 162091) is a condition predisposing to the development of central
and peripheral schwannomas; most cases are sporadic without a clear family history but a …
[PDF] academia.edu

[PDF][PDF] Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

C Bacci, R Sestini, A Provenzano, I Paganini… - Neurogenetics, 2010 - academia.edu
Schwannomatosis (MIM 162091) is a condition predisposing to the development of central
and peripheral schwannomas; most cases are sporadic without a clear family history but a …