Você está em:Start > Publications > View > Síndrome de Frasier- Mutação do gene WT1 como causa de doença do desenvolvimento sexual 46,XY e neuropatia progressiva
Síndrome de Frasier- Mutação do gene WT1 como causa de doença do desenvolvimento sexual 46,XY e neuropatia progressiva
Type
Article in National Scientific Journal
Year
2013
Authors
C Costa
(Author)
Other
The person does not belong to the institution.
The person does not belong to the institution.
The person does not belong to the institution.
Without AUTHENTICUS
Without ORCID
H Pinto
(Author)
Other
The person does not belong to the institution.
The person does not belong to the institution.
The person does not belong to the institution.
Without AUTHENTICUS
Without ORCID
T Martins
(Author)
Other
The person does not belong to the institution.
The person does not belong to the institution.
The person does not belong to the institution.
Without AUTHENTICUS
Without ORCID
J Oliveira
(Author)
Other
The person does not belong to the institution.
The person does not belong to the institution.
The person does not belong to the institution.
Without AUTHENTICUS
Without ORCID