MARÍA ISABEL
TEJADA MÍNGUEZ
Investigadora hasta 2019
Eva
García Alegría
Publicaciones en las que colabora con Eva García Alegría (7)
2009
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Risk of cognitive impairment in female Premutation carriers of fragile X premutation: Analysis by means of robust segmented linear regression models
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 150, Núm. 2, pp. 262-270
2008
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Analysis of the molecular parameters that could predict the risk of manifesting premature ovarian failure in female premutation carriers of fragile X syndrome
Menopause, Vol. 15, Núm. 5, pp. 945-949
2007
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Analysis of FMR1 gene expression in female premutation carriers using robust segmented linear regression models
RNA, Vol. 13, Núm. 5, pp. 756-762
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CHEK2 1100delC is present in familial breast cancer cases of the Basque Country [2]
Breast Cancer Research and Treatment
2006
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Chequeo de mutaciones en el gen BRCA1 en mujeres con cáncer de mama familiar y esporádico precoz, de la Comunidad Autónoma Vasca.
Gaceta médica de Bilbao: Revista oficial de la Academia de Ciencias Médicas de Bilbao. Información para profesionales sanitarios, Vol. 103, Núm. 1, pp. 9-12
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Screening for MECP2 mutations in Spanish patients with an unexplained mental retardation
Clinical Genetics, Vol. 70, Núm. 2, pp. 140-144
2005
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Gene symbol: MECP2. Disease: Rett syndrome (atypical).
Human genetics, Vol. 118, Núm. 3-4, pp. 547