Mowat-Wilson syndrome: Neurological and molecular study in seven patients (2015)
- Authors:
- Autor USP: KIM, CHONG AE - FM
- Unidade: FM
- DOI: 10.1590/0004-282x20140182
- Subjects: DOENÇAS GENÉTICAS; EPILEPSIA; AGENESIA; RETARDO MENTAL
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Arquivos de Neuro-Psiquiatria
- Volume/Número/Paginação/Ano: v. 73, n. 1, p. 12-17, 2015
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by-nc
-
ABNT
PAZ, Jose Albino da; KIM, Chong Ae; GOOSSENS, Michael; GIURGEA, Irina; MARQUES-DIAS, Maria Joaquina. Mowat-Wilson syndrome: Neurological and molecular study in seven patients. Arquivos de Neuro-Psiquiatria, São Paulo, v. 73, n. 1, p. 12-17, 2015. Disponível em: < doi: 10.1590/0004-282X20140182 > DOI: 10.1590/0004-282x20140182. -
APA
Paz, J. A. da, Kim, C. A., Goossens, M., Giurgea, I., & Marques-Dias, M. J. (2015). Mowat-Wilson syndrome: Neurological and molecular study in seven patients. Arquivos de Neuro-Psiquiatria, 73( 1), 12-17. doi:10.1590/0004-282x20140182 -
NLM
Paz JA da, Kim CA, Goossens M, Giurgea I, Marques-Dias MJ. Mowat-Wilson syndrome: Neurological and molecular study in seven patients [Internet]. Arquivos de Neuro-Psiquiatria. 2015 ; 73( 1): 12-17.Available from: doi: 10.1590/0004-282X20140182 -
Vancouver
Paz JA da, Kim CA, Goossens M, Giurgea I, Marques-Dias MJ. Mowat-Wilson syndrome: Neurological and molecular study in seven patients [Internet]. Arquivos de Neuro-Psiquiatria. 2015 ; 73( 1): 12-17.Available from: doi: 10.1590/0004-282X20140182 - Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion
- Remote spinal cord injury in mucopolysaccharidosis type IVA after cervical decompression
- Multimodal image analysis of the retina in Hunter syndrome (mucopolysaccharidosis type II): Case report
- Cognitive and behavioral profile of Williams Syndrome toddlers
- Contribuicao para o estudo da osteogenese imperfeita: aspectos genetico-clinicos de 25 casos
- Estudo genetico e clinico das amiotrofias espinhais progressivas
- Natural history of 39 patients with Achondroplasia
- CBS mutations are good predictors for B6-responsiveness: a study based on the analysis of 35 Brazilian Classical Homocystinuria patients
- NK and B cell deficiency in a MPS type II family with novel mutation in the IDS gene
- Diagnosis and management of classica homocystinuria in Brazil: a summary of 72 late-diagnosed patients
Informações sobre o DOI: 10.1590/0004-282x20140182 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
