M. Jiménez-Sáinz

Centric fission, centromere‐telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomy

J. Cantú, H. Rivera, G. Vaca, 1987, Clinical genetics.

Azoospermia and duplication 3qter as distinct consequences of a familial t(X;3) (q26;q13.2).

J. Cantú, H. Rivera, M. Díaz, 1985, American journal of medical genetics.

Type and contretype signs in monosomy and trisomy 9p. On a case 46,XY, del (9) (pter yields p12:).

J. Cantú, H. Rivera, A. Hernández, 1979, Annales de genetique.

[Chromosome aberrations in 334 individuals with various types of abortion (including 144 couples)].

J. Cantú, H. Rivera, A. Hernández, 1985, Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion.

Monosomy 20p due to a de novo del(20)(p12.2). Clinical and radiological delineation of the syndrome.

J. Śanchez-Corona, J. Cantú, H. Rivera, 1985, Annales de genetique.

Whole‐arm t (X;17) (Xp17q;Xq17p) and gonadal dysgenesis

J. Cantú, H. Rivera, A. Rolón, 1986, Clinical genetics.