Canlyniadau Chwilio - Stabile, M

A case of suspected teratogenic holoprosencephaly. gan Stabile, M, Bianco, A, Iannuzzi, S, Buonocore, M C, Ventruto, V

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Autosomal dominant inheritance of Gerhardt's syndrome in three generations of a family. gan Morelli, G, Mesolella, C, Cavaliere, M L, Stabile, M, Ventruto, V

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Primary protrusio acetabuli in four generations of an Italian family. gan Ventruto, V, Stabile, M, Cavaliere, M L, Pagano, L, Fioretti, G, Celona, A

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Multiple endocrine neoplasia type 2 (Sipple's syndrome): clinical and cytogenetic analysis of a kindred. gan Zatterale, A, Stabile, M, Nunziata, V, Di Giovanni, G, Vecchione, R, Ventruto, V

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Prune belly appearance in a Turner subject. gan Savanelli, A, Orfeo, L, Stabile, M, Iannuzzi, S, De Bellis, U, Esposito, G, Ventruto, V

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Ring (13),t(2;6) associated with familial fragile (16). gan Ventruto, V, Rinaldi, A, Renda, S, Stabile, M, Rinaldi, M M, Cavaliere, M L, Conte, N, Aveta, V

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Study of a form of pulverulent cataract in a large kindred. gan Stabile, M, Amoriello, A, Capobianco, S, Cavaliere, M L, Conte, N, De Rosa, C, Ruoppo, S, Sorrentino, V, Ventruto, V

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Mapping of a locus for a familial autosomal recessive idiopathic myoclonic epilepsy of infancy to chromosome 16p13. gan Zara, F, Gennaro, E, Stabile, M, Carbone, I, Malacarne, M, Majello, L, Santangelo, R, de Falco, F A, Bricarelli, F D

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Mental retardation and cardiovascular malformations in NF1 microdeleted patients point to candidate genes in 17q11.2 gan Venturin, M, Guarnieri, P, Natacci, F, Stabile, M, Tenconi, R, Clementi, M, Hernandez, C, Thompson, P, Upadhyaya, M, Larizza, L, Riva, P

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