R. Martínez y Martínez

Clinical features in the Wiedemann-Beckwith syndrome.

R. Martínez y Martínez, 1996, Clinical genetics.

The Wiedemann-Beckwith syndrome in four sibs including one with associated congenital hypothyroidism

J. Cantú, R. Ocampo-Campos, R. Martínez y Martínez, 2004, European Journal of Pediatrics.

Autosomal dominant macroglossia in two unrelated families

J. Cantú, A. Hernández, M. C. Reynoso, 1986, Human Genetics.

The 22q distal trisomy syndrome in a recombinant child.

G. Pérez-García, R. Martínez y Martínez, H. Rivera, 1988, Annales de genetique.

49,XXXXX syndrome.

J. Cantú, A. Hernández, R. Fragoso, 1982, Annales de genetique.

Malformed genitalia in the 47,XYY genotype.

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