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Genetic aspects of adolescent idiopathic scoliosis in a family with multiple affected members: a research article.
Published in:
Scoliosis (17487161), 2010, v. 5, p. 7, doi. 10.1186/1748-7161-5-7
By:
- Wajchenberg, Marcelo;
- Lazar, Monize;
- Cavaçana, Natale;
- Martins, Delio Eulalio;
- Licinio, Luciana;
- Puertas, Eduardo Barros;
- Landim, Elcio;
- Zatz, Mayana;
- Ishida, Akira
Publication type:
Article
Spastic Paraplegia, Optic Atrophy, and Neuropathy: New Observations, Locus Refinement, and Exclusion of Candidate Genes.
Published in:
Annals of Human Genetics, 2009, v. 73, n. 3, p. 382, doi. 10.1111/j.1469-1809.2009.00507.x
By:
- Macedo-Souza, Lúcia Inês;
- Kok, Fernando;
- Santos, Silvana;
- Licinio, Luciana;
- Lezirovitz, Karina;
- Cavaçana, Natale;
- Bueno, Clarissa;
- Amorim, Simone;
- Pessoa, André;
- Graciani, Zodja;
- Ferreira, Áurea;
- Prazeres, Abdísio;
- de Melo, Áurea Nogueira;
- Otto, Paulo Alberto;
- Zatz, Mayana
Publication type:
Article
A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G).
Published in:
Human Molecular Genetics, 2014, v. 23, n. 15, p. 4103, doi. 10.1093/hmg/ddu127
By:
- Vieira, Natássia M.;
- Naslavsky, Michel S.;
- Licinio, Luciana;
- Kok, Fernando;
- Schlesinger, David;
- Vainzof, Mariz;
- Sanchez, Nury;
- Kitajima, João Paulo;
- Gal, Lihi;
- Cavaçana, Natale;
- Serafini, Peter R.;
- Chuartzman, Silvia;
- Vasquez, Cristina;
- Mimbacas, Adriana;
- Nigro, Vincenzo;
- Pavanello, Rita C.;
- Schuldiner, Maya;
- Kunkel, Louis M.;
- Zatz, Mayana
Publication type:
Article
Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25.
Published in:
2008
By:
- Macedo-Souza, Lúcia;
- Kok, Fernando;
- Santos, Silvana;
- Licinio, Luciana;
- Lezirovitz, Karina;
- Nascimento, Rafaella;
- Bueno, Clarissa;
- Martyn, Marcília;
- Leão, Emília;
- Zatz, Mayana
Publication type:
Letter

Found: 4

Genetic aspects of adolescent idiopathic scoliosis in a family with multiple affected members: a research article.

Spastic Paraplegia, Optic Atrophy, and Neuropathy: New Observations, Locus Refinement, and Exclusion of Candidate Genes.

A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G).

Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25.