Protein and DNA Analysis for the Prenatal Diagnosis of α2-Laminin–Deficient Congenital Muscular Dystrophy von Yamamoto, Lydia U, Gollop, Thomas R, Naccache, Nadyr F, Pavanello, Rita C. M, Zanoteli, Edmar, Zatz, Mayana, Vainzof, Mariz

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Protein and DNA analysis for the prenatal diagnosis of alpha2-laminin-deficient congenital muscular dystrophy von Yamamoto, Lydia U, Gollop, Thomas R, Naccache, Nadyr F, Pavanello, Rita C M, Zanoteli, Edmar, Zatz, Mayana, Vainzof, Mariz

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Prenatal diagnosis of 48,XYY, + 21 ascertained through ultrasound anomalies von Gollop, Thomaz Rafael, Naccache, Nadyr F., Auler-Bittencourt, Eloisa, Hauschild, Decio, Eigier, Alberto, Zveibil, Deborah K.

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Duplication of distal 17q: Report of an observation von Naccache, Nadyr F., Vianna-Morgante, Angela M., Richieri-Costa, A., Opitz, John M.

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