ReP USP - Resultado da busca

Artigo de periodico
Diagnosis of limb-girdle muscular dystrophy 2A by immunohistochemical techniques (2008)
Kolski, Hanna K; Hawkins, Cynthia; Zatz, Mayana ; Paula, Flavia de; Biggar, Doug; Alman, Ben; Vajsar, Jiri
Source: Neuropathology. Unidade: IB
Subjects: IMUNOHISTOQUÍMICA, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KOLSKI, Hanna K et al. Diagnosis of limb-girdle muscular dystrophy 2A by immunohistochemical techniques. Neuropathology, v. 28, n. Ju 2008, p. 264-268, 2008Tradução . . Disponível em: https://doi.org/10.1111/j.1440-1789.2007.00871.x. Acesso em: 18 ago. 2024.
APA
Kolski, H. K., Hawkins, C., Zatz, M., Paula, F. de, Biggar, D., Alman, B., & Vajsar, J. (2008). Diagnosis of limb-girdle muscular dystrophy 2A by immunohistochemical techniques. Neuropathology, 28( Ju 2008), 264-268. doi:10.1111/j.1440-1789.2007.00871.x
NLM
Kolski HK, Hawkins C, Zatz M, Paula F de, Biggar D, Alman B, Vajsar J. Diagnosis of limb-girdle muscular dystrophy 2A by immunohistochemical techniques [Internet]. Neuropathology. 2008 ; 28( Ju 2008): 264-268.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1111/j.1440-1789.2007.00871.x
Vancouver
Kolski HK, Hawkins C, Zatz M, Paula F de, Biggar D, Alman B, Vajsar J. Diagnosis of limb-girdle muscular dystrophy 2A by immunohistochemical techniques [Internet]. Neuropathology. 2008 ; 28( Ju 2008): 264-268.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1111/j.1440-1789.2007.00871.x
Trabalho de evento
Nemaline myopathy (NM) in brazilian patients (1998)
Gurgel, J E P; Reed, Umbertina Conti; Carvalho, M. S.; Marie, Suely Kazue Nagahashi; Zatz, Mayana ; Vainzof, Mariz
Conference titles: Meeting of the International Congress of Neuromuscular Diseases. Unidades: FM, IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GURGEL, J E P et al. Nemaline myopathy (NM) in brazilian patients. 1998, Anais.. Adelaide: Faculdade de Medicina, Universidade de São Paulo, 1998. . Acesso em: 18 ago. 2024.
APA
Gurgel, J. E. P., Reed, U. C., Carvalho, M. S., Marie, S. K. N., Zatz, M., & Vainzof, M. (1998). Nemaline myopathy (NM) in brazilian patients. In . Adelaide: Faculdade de Medicina, Universidade de São Paulo.
NLM
Gurgel JEP, Reed UC, Carvalho MS, Marie SKN, Zatz M, Vainzof M. Nemaline myopathy (NM) in brazilian patients. 1998 ;[citado 2024 ago. 18 ]
Vancouver
Gurgel JEP, Reed UC, Carvalho MS, Marie SKN, Zatz M, Vainzof M. Nemaline myopathy (NM) in brazilian patients. 1998 ;[citado 2024 ago. 18 ]
Trabalho de evento-resumo
The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis (1998)
Zatz, Mayana ; Marie, Suely Kazue Nagahashi; Cerqueira, Antonia Maria Pereira; Vainzof, Mariz ; Pavanello, Rita de Cássia M; Passos-Bueno, Maria Rita
Source: Conference Handbook and Speaker Papers. Conference titles: Facioscapulohumeral Muscular Dystrophy Meeting. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis. 1998, Anais.. Sydney: Instituto de Biociências, Universidade de São Paulo, 1998. . Acesso em: 18 ago. 2024.
APA
Zatz, M., Marie, S. K. N., Cerqueira, A. M. P., Vainzof, M., Pavanello, R. de C. M., & Passos-Bueno, M. R. (1998). The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis. In Conference Handbook and Speaker Papers. Sydney: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Marie SKN, Cerqueira AMP, Vainzof M, Pavanello R de CM, Passos-Bueno MR. The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis. Conference Handbook and Speaker Papers. 1998 ;[citado 2024 ago. 18 ]
Vancouver
Zatz M, Marie SKN, Cerqueira AMP, Vainzof M, Pavanello R de CM, Passos-Bueno MR. The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis. Conference Handbook and Speaker Papers. 1998 ;[citado 2024 ago. 18 ]

USP Schools

ReP

Filtros

Authors