G. Castiñeyra

发表

Molecular, Cytogenetic, Hormonal and Clinical Characterization of Ten XX Males Including Genetic Counseling

C. Perandones, G. Castiñeyra, S. Copelli, 2001 .

46,XX MALE: CLINICAL, HORMONAL/GENETIC FINDINGS

O. Levalle, G. Castiñeyra, S. Copelli, 2002, Archives of andrology.

Fetal phenotype in a case of partial trisomy 21 and partial monosomy 22 detected prenatally.

R. Coco, J. M. Sánchez, T. C. de Negrotti, 1981, Journal of Medical Genetics.

Two sibs with Wiedemann-Rautenstrauch syndrome: possibilities of prenatal diagnosis by ultrasound.

E. Goldschmidt, J. M. Sánchez, G. Castiñeyra, 1992, Journal of medical genetics.