Facioscapulohumel muscular dystrophy: gender differences and genetic counselling in a complex disorder (2004)
- Authors:
- Autor USP: ZATZ, MAYANA - IB
- Unidade: IB
- Subjects: DISTROFIA MUSCULAR; DOENÇAS GENÉTICAS
- Language: Inglês
- Imprenta:
- Publisher: BIOS Scientific Publishers
- Publisher place: London
- Date published: 2004
- Source:
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ABNT
TONINI, Maria Manuela de Oliveira; ZATZ, Mayana. Facioscapulohumel muscular dystrophy: gender differences and genetic counselling in a complex disorder. In: FSHD facioscapulohumel muscular dystrophy: clinical medicine and molecular cell biology[S.l: s.n.], 2004. -
APA
Tonini, M. M. de O., & Zatz, M. (2004). Facioscapulohumel muscular dystrophy: gender differences and genetic counselling in a complex disorder. In FSHD facioscapulohumel muscular dystrophy: clinical medicine and molecular cell biology. London: BIOS Scientific Publishers. -
NLM
Tonini MM de O, Zatz M. Facioscapulohumel muscular dystrophy: gender differences and genetic counselling in a complex disorder. In: FSHD facioscapulohumel muscular dystrophy: clinical medicine and molecular cell biology. London: BIOS Scientific Publishers; 2004. -
Vancouver
Tonini MM de O, Zatz M. Facioscapulohumel muscular dystrophy: gender differences and genetic counselling in a complex disorder. In: FSHD facioscapulohumel muscular dystrophy: clinical medicine and molecular cell biology. London: BIOS Scientific Publishers; 2004. - Distrofia miotônica e cardiopatia: comportamento dos eventos arrítmicos e dos distúrbios da condução
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- E o hormônio de crescimento normal na distrofia de Duchenne (DMD)?
- Mazindol and growth-hormone (gh) in duchenne dystrophy
- Serum creatine kinase and pyruvate kinase levels in females of different racial background at risks for duchenne muscular dystrophy
- Assesment in double blind test of a drug therapy in monozygotic twins affected with Duchenne muscular dystrophy (DMD)
- Age effect on serum creatine-kinase (ck) and pyruvate-kinase (pk) in carriers of duchenne muscular dystrophy (dmd) gene: a follow-up study
- Atividade de enzima isocitrato desidrogenase no soro sanguíneo de heterozigotas certas quanto ao gene da distrofia tipo duchenne (dm)
- Estudos de fragmentos de restricao em mulheres de diferentes grupos raciais pertencentes a familias com afetados por distrofia muscular de duchenne (dmd) e becker (dmb)
- Crescimento em afetados pela distrofia muscular de duchenne (dmd)
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