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Descripción cito genética de las líneas celulares de anemia de Fanconi pertenecientes a los grupos de complementación a (HSC72), D2 (PD20) y una línea normal (6846). /Cytogenetic description of the fanconi anemia cell lines belonging to complementation groups a (HSC72), D2 (PD20) and a normal line (6846).

PALOMA DEL CARMEN NERI VIDAURRI (El Autor, 2004)

Fanconi Anemia and Laron Syndrome

Rocio García De la Garza; Gabriel Amador Aguirre; Mariano García-Magariño Alonso; María Inmaculada Castilla de Cortázar Larrea; Julieta Rodríguez de Ita; Fabiola Castorena Torres; Martha Irma Elizondo Leal

Apoptosis and expression of anti- andpro-apoptotic proteins in peripheral blood mononuclear cells of Fanconi anaemia patients: a study of 73 cases

Baruque, Graça A.; Bitencourt, M. A.; Pasquini, Ricardo; Castelo-Branco, Morgana T. L; Llerena Junior, Juan Clinton; Rumjanek, Vivian M. (2010)

Molecular analysis of the most prevalent mutations of the FANCA and FANCC genes in Brazilian patients with Fanconi anaemia

Rodriguez, David Enrique Aguilar; Lima, Carmen Silvia Passos; Lourenço, Gustavo Jacob; Figueiredo, Maria Estela; Carneiro, Jorge David Aivazoglu; Tone, Luiz Gonzaga; Llerena Junior, Juan Clinton; Toscano, Raquel Alves; Brandalise, Silvia; Pinto Júnior, Walter; Costa, Fernando Ferreira; Bertuzzo, Carmen Sílvia (2010)

An update on Fanconi anemia: Clinical, cytogenetic and molecular approaches (Review)

Moreno Niño, Olga María; Paredes Brijaldo, Angela Camila; Suárez-Obando, F.; Rojas, Adriana (2022)

Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de FanconiMolecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia

Gonçalves, Claudia Estela, 1970- ([s.n.], 2014)

Pediatric Dental Care in Fanconi Anemia: A Case Report

Gaitán-Fonseca,César; Frías-Muñoz;,Maribel; Guerrero-de la Torre,Luis Enrique; Lemus-Rojero,Obed,; Aguilera-Galavíz,Luis Alejandro, (Facultad de Odontología. Universidad de Costa Rica, 2018)

Molecular analysis of the most prevalent mutations of the FANCA and FANCC genes in Brazilian patients with Fanconi anaemia

An update on Fanconi anemia: Clinical, cytogenetic and molecular approaches (Review)

Moreno Niño, Olga María; Paredes Brijaldo, Angela Camila; Suárez-Obando, F.; Rojas, Adriana

Fanconi anemia is a genetic syndrome clinically characterized by congenital malformations that affect several human systems, leads to progressive bone marrow failure and predisposes an individual to cancer, particularly ...

Estudo das mutações do gene FANCG em pacientes com quadro clinico sugestivo de anemia de FanconiMutation analysis of FANCG gene in patients with compatible clinical to Fanconi anaemia

Amstalden, Lucila Gobby ([s.n.], 2006)

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Filtros

Fanconi Anemia and Laron Syndrome

Apoptosis and expression of anti- andpro-apoptotic proteins in peripheral blood mononuclear cells of Fanconi anaemia patients: a study of 73 cases

Molecular analysis of the most prevalent mutations of the FANCA and FANCC genes in Brazilian patients with Fanconi anaemia

An update on Fanconi anemia: Clinical, cytogenetic and molecular approaches (Review)

Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de FanconiMolecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia

Pediatric Dental Care in Fanconi Anemia: A Case Report

Molecular analysis of the most prevalent mutations of the FANCA and FANCC genes in Brazilian patients with Fanconi anaemia

An update on Fanconi anemia: Clinical, cytogenetic and molecular approaches (Review)

Estudo das mutações do gene FANCG em pacientes com quadro clinico sugestivo de anemia de FanconiMutation analysis of FANCG gene in patients with compatible clinical to Fanconi anaemia