Phenotypic variation of a new P0 mutation in genetically identical twins (1998)
- Authors:
- Autor USP: MARQUES JUNIOR, WILSON - FMRP
- Unidade: FMRP
- Subjects: NEUROPEDIATRIA; TRANSTORNOS CEREBROVASCULARES
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts
- Conference titles: International Conference on Charcot-Marie-Tooth Disorders
-
ABNT
MARQUES JÚNIOR, Wilson et al. Phenotypic variation of a new P0 mutation in genetically identical twins. 1998, Anais.. Quebec: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 1998. . Acesso em: 29 dez. 2025. -
APA
Marques Júnior, W., Hanna, M. G., Marques, S. R., Sweeney, M. G., Thomas, P. K., & Wood, N. W. (1998). Phenotypic variation of a new P0 mutation in genetically identical twins. In Abstracts. Quebec: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Marques Júnior W, Hanna MG, Marques SR, Sweeney MG, Thomas PK, Wood NW. Phenotypic variation of a new P0 mutation in genetically identical twins. Abstracts. 1998 ;[citado 2025 dez. 29 ] -
Vancouver
Marques Júnior W, Hanna MG, Marques SR, Sweeney MG, Thomas PK, Wood NW. Phenotypic variation of a new P0 mutation in genetically identical twins. Abstracts. 1998 ;[citado 2025 dez. 29 ] - Potencial de acao sensitivo do nervo mediano com eletrodos de agulha justapostos ao nervo na hanseniase virchowiana e dimorfo-virchowiana
- Phenotypic manifestations of chromosome 17 p112 duplication
- Dorsal cutaneous nerve conductions study in normal subjects
- Leprosy neuropathy
- Reflexo cutâneo plantar em extensão: sinal de Babinski
- New mutations in the ATM gene and clinical data of 25 AT patients
- Postsurgical idiopathic brachial neuritis
- Does pregnancy change the natural history of CMT1A neuropathy ?
- Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis
- Repeat expansion size predicts age of onset in rfc1 canvas and disease spectrum
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas