MARÍA ISABEL
TEJADA MÍNGUEZ
Ikertzailea 2019-(e)ra arte
Vall d'Hebron Institut de Recerca
Barcelona, EspañaVall d'Hebron Institut de Recerca-ko ikertzaileekin lankidetzan egindako argitalpenak (2)
2020
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Role of mitochondrial DNA variants in the development of fragile X-associated tremor/ataxia syndrome
Mitochondrion, Vol. 52, pp. 157-162
2013
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Trisomy 18p caused by a supernumerary marker with a chromosome 13/21 centromere: A possible recurrent chromosome aberration
American Journal of Medical Genetics, Part A, Vol. 161, Núm. 9, pp. 2363-2368