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G.P.40 LGMD2G with clinical presentation of congenital muscular dystrophy: A rare phenotype

✍ Scribed by Almeida, C.F.; Lima, B.L.; Onofre-Oliveira, P.C.G.; Pavanello, R.C.M.; Zatz, M.; Vainzof, M.

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📜 SIMILAR VOLUMES

G.P.14.12 Phenotype of three putative no

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G.P.2.02 Genotype–phenotype correlations

✍ S.M. Messina; F.M.S. Santorelli; M.M. Mora; C.B. Bruno; E.P. Pegoraro; A.P. Pini 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 46 KB

G.P.4.01 Rare congenital presentation of

✍ L. Medne; A. Glanzman; J. Flickinger; T. Estilow; M. Rozenberg; C. Bönnemann 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 46 KB

G.P.2.01 Frequency of different forms of

✍ B. Talim; Z. Akcoren; G. Haliloglu; D. Orhan; S. Gucer; G. Kale; H. Topaloglu 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 46 KB

Clinical phenotype in congenital muscula

✍ J. Philpot; C. Sewry; J. Pennock; V. Dubowitz 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 361 KB

G.P.13.06 Clinical phenotype of Becker m

✍ C.S.M. Straathof; A.T.J. Helderman-van den Enden; A. Aartsma-Rus; J.T. den Dunne 📂 Article 📅 2009 🏛 Elsevier Science 🌐 English ⚖ 39 KB