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	1.	Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. [electronic resource] by Moreira, E S Vainzof, M Suzuki, O T Pavanello, R C M Zatz, M Passos-Bueno, M R Producer: 20030310 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Milder course in Duchenne patients with nonsense mutations and no muscle dystrophin. [electronic resource] by Zatz, M Pavanello, R C M Lazar, M Yamamoto, G L Lourenço, N C V Cerqueira, A Nogueira, L Vainzof, M Producer: 20150720 In: Neuromuscular disorders : NMD vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. [electronic resource] by Abe, K T Lino, A M M Hirata, M T A Pavanello, R C M Brotto, M W I Marchiori, P E Zatz, M Producer: 20040621 In: Neuromuscular disorders : NMD vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype. [electronic resource] by Tonini, M M O Pavanello, R C M Gurgel-Giannetti, J Lemmers, R J van der Maarel, S M Frants, R R Zatz, M Producer: 20040223 In: Journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)