M. Baena

发表

Identification of 31 novel mutations in the F8 gene in Spanish hemophilia A patients: structural analysis of 20 missense mutations suggests new intermolecular binding sites.

M. Baiget, E. Tizzano, A. Venceslá, 2008, Blood.

suggests new intermolecular binding sites hemophilia A patients: structural analysis of 20 missense mutations Identification of 31 novel mutations in the F8 gene in Spanish

M. Baiget, E. Tizzano, A. Venceslá, 2013 .

BRCA 2 mutation analysis of 87 Spanish breast / ovarian cancer families

C. Alonso, O. Díez, M. Baiget, 2005 .

BRCA2 mutation analysis of 87 Spanish breast/ovarian cancer families.

C. Alonso, O. Díez, M. Baiget, 2001, Annals of oncology : official journal of the European Society for Medical Oncology.

A Single-Nucleotide Polymorphism in the Aromatase Gene Is Associated with the Efficacy of the Aromatase Inhibitor Letrozole in Advanced Breast Carcinoma

B. Lloveras, I. Tusquets, M. Monzó, 2008, Clinical Cancer Research.

High Mutational Heterogeneity, and New Mutations in the Human Coagulation Factor V Gene. Future Perspectives for Factor V Deficiency Using Recombinant and Advanced Therapies

E. Tizzano, M. Baena, L. Alías, 2021, International journal of molecular sciences.

Clinical and genetic findings in five female patients with haemophilia A: Identification of a novel missense mutation, p.Phe2127Ser

E. Tizzano, V. Jiménez‐Yuste, M. Álvarez‐Román, 2010, Thrombosis and Haemostasis.

First report of two independent point factorVIII mutations in a family with haemophilia a: a word of caution for carrier diagnosis.

M. Baiget, E. Tizzano, R. Pérez Garrido, 2005, Thrombosis and Haemostasis.

Rapid identification of female haemophilia A carriers with deletions in the factor VIII gene by quantitative Real-Time PCR analysis

M. Barceló, M. Baiget, E. Tizzano, 2005, Thrombosis and Haemostasis.

F8 gene dosage defects in atypical patients with severe haemophilia A

J. Rosell, M. Baiget, E. Tizzano, 2012, Haemophilia : the official journal of the World Federation of Hemophilia.

Severe haemophilia A in a female resulting from an inherited gross deletion and a de novo codon deletion in the F8 gene

M. Baiget, E. Tizzano, M. Quintana, 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

Marker and real-time quantitative analyses to confirm hemophilia B carrier diagnosis of a complete deletion of the F9 gene

M. Barceló, M. Baiget, E. Tizzano, 2007, Haematologica.

Application of intron 9 and intron 25 dinucleotide repeats of the factor VIII gene for carrier diagnosis in haemophilia A

M. Baiget, E. Tizzano, A. Venceslá, 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

Utility of a (GT)n dinucleotide repeat in intron 1 of the factor 8 gene for haemophilia A carrier diagnosis

M. Baiget, E. Tizzano, A. Venceslá, 2005, Haemophilia : the official journal of the World Federation of Hemophilia.

DMD Mutations in 576 Dystrophinopathy Families: A Step Forward in Genotype-Phenotype Correlations

M. Baiget, C. Ortez, J. Juan-Mateu, 2015, PloS one.

Mutations in the NKX2-5 gene in patients with stroke and patent foramen ovale

F. Carreras, J. Martí-Fàbregas, M. Baiget, 2009, Clinical Neurology and Neurosurgery.

RNA analysis of eight BRCA1 and BRCA2 unclassified variants identified in breast/ovarian cancer families from Spain

C. Alonso, O. Díez, M. Baiget, 2003, Human mutation.

The R71G BRCA1 is a founder Spanish mutation and leads to aberrant splicing of the transcript

N. Janin, C. Alonso, O. Díez, 2001, Human mutation.