G. Croci

发表

The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications.

G. Gimelli, G. Floridia, O. Zuffardi, 1996, American journal of human genetics.

Frequency of consanguineous marriages among parents and grandparents of Down patients

M. Devoto, R. Tenconi, L. Zelante, 2004, Human Genetics.

Parental mosaicism in de novo translocation (21q21q) Down's syndrome.

F. Franchi, G. Croci, 1991, Journal of medical genetics.

BrdU-sensitive fragile site on long arm of chromosome 16.

G. Croci, 1983, American journal of human genetics.

Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: a study of 87 families.

L. Zelante, C. Lo Nigro, L. Perroni, 1996, American journal of medical genetics.

MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literature.

J. Clayton-Smith, J. Hurst, L. Garavelli, 2005, Genetic counseling.

Tetrasomy 9p confirmed by GALT.

F. Franchi, G. Giovannelli, P. Balestrazzi, 1983, Journal of medical genetics.

Dermatologic Features in Pallister–Killian Syndrome and their Importance to the Diagnosis

L. Garavelli, F. Franchi, S. Amarri, 2007, Pediatric dermatology.

Therapy of advanced acute myeloblastic leukemia with cytarabine and interleukin 2.

M. Santucci, A. Castriota Scanderbeg, A. Butturini, 1991, Leukemia research.

A familial case of chromosome 16p variant.

L. Camurri, F. Franchi, G. Croci, 1991, Journal of medical genetics.

Anophthalmos with limb anomalies (Waardenburg opththalmo-acromelic syndrome): report of a new Italian case with renal anomaly and review.

L. Garavelli, A. Superti-Furga, A. Ammenti, 2006, Genetic counseling.