Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo de Congresso
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Is autosomal dominat nonsyndromic deafness in a Brazilian pedigree linked to DFNA7/DFNM1?Karina Lezirovitz M. C. C Braga; Paulo A Otto; Regina Celia Mingroni Netto; Annual Meeting of the American Society of Human Genetics (52. 2002 Baltimore)Abstracts v. 71, n. 4, suppl., p. 440 res.1575, oct. 2002Baltimore 2002Item não circula. Consulte sua biblioteca.(Acessar) |
2 |
Material Type: Artigo de Congresso
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Size of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring implications for the origin of mosaicismRegina Celia Mingroni Netto Luciana Amaral Haddad; Angela M Vianna-Morgante; International Workshop on the Fragile X and X-Linked Mental Retardation (7. 1995 Tromso)Abstracts 1995Tromso 1995Item não circula. Consulte sua biblioteca.(Acessar) |
3 |
Material Type: Artigo de Congresso
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X-inactivation in fragile-X carriersAngela M Vianna-Morgante S. S Costa; Paulo A Otto; Regina Celia Mingroni Netto; International Workshop on Fragile X and X-Linked Mental Retardation (9. 1999 Strasbourg)Abstracts Strasbourg, 1999Strasbourg 1999Item não circula. Consulte sua biblioteca.(Acessar) |
4 |
Material Type: Artigo de Congresso
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Simple and non- isotopic pcr - based diagnostic test suitable for population screening of fragil x syndrome among mentally handicapped menLuciana Amaral Haddad Regina Celia Mingroni Netto; Angela M Vianna-Morgante; S D J Pena; International Workshop on the Fragile X and X-Linked Mental Retardation (7. 1995 Tromso)Abstracts 1995Tromso 1995Item não circula. Consulte sua biblioteca.(Acessar) |
5 |
Material Type: Artigo de Congresso
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Distribution of CGG repeats and FRAXAC1/DXS548 alleles in brazilian populationsRegina Celia Mingroni Netto Claudia Blanes Angeli; M T B M Auricchio; E R L Mesquita; M N K Guimarães; Angela M Vianna-Morgante; International Workshop on Fragile X and X-Linked Mental Retardation (9. 1999 Strasbourg)Abstracts Strasbourg, 1999Strasbourg 1999Item não circula. Consulte sua biblioteca.(Acessar) |
6 |
Material Type: Artigo de Congresso
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Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian familyRegina Celia Mingroni Netto V. G. L Dantas; E.L Freitas; A. M. S. M Moraes; M. C. C Braga; S. B Ramos; Carla Rosenberg; V.A Della-Rosa; Annual Meeting of the American Society of Human Genetics 2013 BostonAbstracts Boston, 2013Boston 2014Acesso online |