Down syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21) (q26;q22.1) by FISH.

Por Nadal, M, Moreno, S, Pritchard, M, Preciado, M A, Estivill, X, Ramos-Arroyo, M A
Publicado em 1997

Hereditary neuropathy with liability to pressure palsies: two cases with a reciprocal translocation t(16;17)(q12;p11.2) interrupting the PMP22 gene

Por NADAL, M., VALIENTE, A., DOMENECH, A., PRITCHARD, M., ESTIVILL, X., RAMOS-ARROYO, M. A.
Publicado em 2000

A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.

Por Bayés, M, Goldaracena, B, Martínez-Mir, A, Iragui-Madoz, M I, Solans, T, Chivelet, P, Bussaglia, E, Ramos-Arroyo, M A, Baiget, M, Vilageliu, L, Balcells, S, Gonzàlez-Duarte, R, Grinberg, D
Publicado em 1998

Repeat Instability in the 27–39 CAG Range of the HD Gene in the Venezuelan Kindreds: Counseling Implications

Por Brocklebank, D., Gayán, J., Andresen, J.M., Roberts, S.A., Young, A.B., Snodgrass, S.R., Penney, J.B., Ramos-Arroyo, M.A., Cha, J.J., Rosas, H.D., Hersch, S.M., Feigin, A., Cherny, S.S., Wexler, N.S., Housman, D.E., Cardon, L.R.
Publicado no Am J Med Genet B Neuropsychiatr Genet (2009)