An illustrative case of neurofibromatosis type 1 and NF1 microdeletion (2010)
- Authors:
- USP affiliated authors: COSTA, SILVIA SOUZA DA - IB ; MORGANTE, ANGELA MARIA VIANNA - IB ; OTTO, PAULO ALBERTO - IB
- Unidade: IB
- Subjects: NEUROFIBROMATOSES; GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Molecular Syndromology
- ISSN: 1661-8769
- Volume/Número/Paginação/Ano: v. 1, n. 3, p. 133-135, 2010
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ABNT
PRAXEDES, Leide de Almeida et al. An illustrative case of neurofibromatosis type 1 and NF1 microdeletion. Molecular Syndromology, v. 1, n. 3, p. 133-135, 2010Tradução . . Acesso em: 03 out. 2024. -
APA
Praxedes, L. de A., Pereira, F. M., Mazzeu, J. F., Costa, S. S. da, Bertola, D. R., Kim, C. A., et al. (2010). An illustrative case of neurofibromatosis type 1 and NF1 microdeletion. Molecular Syndromology, 1( 3), 133-135. -
NLM
Praxedes L de A, Pereira FM, Mazzeu JF, Costa SS da, Bertola DR, Kim CA, Vianna-Morgante AM, Otto PA. An illustrative case of neurofibromatosis type 1 and NF1 microdeletion. Molecular Syndromology. 2010 ; 1( 3): 133-135.[citado 2024 out. 03 ] -
Vancouver
Praxedes L de A, Pereira FM, Mazzeu JF, Costa SS da, Bertola DR, Kim CA, Vianna-Morgante AM, Otto PA. An illustrative case of neurofibromatosis type 1 and NF1 microdeletion. Molecular Syndromology. 2010 ; 1( 3): 133-135.[citado 2024 out. 03 ] - PLP1 duplication at the breakpoint regions of an apparently balanced t(X,22) translocation causes Pelizaeus-Merzbacher disease in a girl
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