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TP53 p.R337H prevalence in a series of Brazilian hereditary breast cancer families.
Published in:
Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-8
By:
- Cury, Nathalia M.;
- Ferraz, Victor E. F.;
- Silva Jr, Wilson A.
Publication type:
Article
Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS-FREM complex disorders.
Published in:
American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 12, p. 3012, doi. 10.1002/ajmg.a.36119
By:
- Schanze, Denny;
- Harakalova, Magdalena;
- Stevens, Cathy A.;
- Brancati, Francesco;
- Dallapiccola, Bruno;
- Farndon, Peter;
- Ferraz, Victor E. F.;
- McDonald‐McGinn, Donna M.;
- Zackai, Elaine H.;
- Wright, Michael;
- van Lieshout, Stef;
- Vogel, Maartje J.;
- van Haelst, Mieke M.;
- Zenker, Martin
Publication type:
Article
Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil.
Published in:
PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0127147
By:
- de Melo, Mônica Barbosa;
- Mandal, Anil K.;
- Tavares, Ivan M.;
- Ali, Mohammed Hasnat;
- Kabra, Meha;
- de Vasconcellos, José Paulo Cabral;
- Senthil, Sirisha;
- Sallum, Juliana M. F.;
- Kaur, Inderjeet;
- Betinjane, Alberto J.;
- Moura, Christiane R.;
- Paula, Jayter S.;
- Costa, Karita A.;
- Sarfarazi, Mansoor;
- Paolera, Mauricio Della;
- Finzi, Simone;
- Ferraz, Victor E. F.;
- Costa, Vital P.;
- JrBelfort, Rubens;
- Chakrabarti, Subhabrata
Publication type:
Article
Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN).
Published in:
2022
By:
- Félix, Têmis Maria;
- de Oliveira, Bibiana Mello;
- Artifon, Milena;
- Carvalho, Isabelle;
- Bernardi, Filipe Andrade;
- Schwartz, Ida V. D.;
- Saute, Jonas A.;
- Ferraz, Victor E. F.;
- Acosta, Angelina X.;
- Sorte, Ney Boa;
- Alves, Domingos;
- RARAS Network group;
- Amorim, Tatiana;
- Adjuto, Gisele Maria Araujo Felix;
- Almeida, Rosemarie Elizabeth Schimidt;
- Brandão, Flávia Resedá;
- Bueno, Larissa Souza Mario;
- de Andrade, Maria Denise Fernandes Carvalho;
- Cagliari, Cristina Iacovelo;
- Cardoso, Maria Terezinha
Publication type:
journal article

Found: 4

TP53 p.R337H prevalence in a series of Brazilian hereditary breast cancer families.

Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS-FREM complex disorders.

Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil.

Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN).