M. P. Vardeu

Short rib-dysplasia group (with/without polydactyly): report of a patient suggesting the existence of a continuous spectrum.

A. Guala, P. Franceschini, D. Franceschini, 1995, American journal of medical genetics.

Variability of clinical and immunological phenotype in immunodeficiency-centromeric instability-facial anomalies syndrome

A. Guala, P. Tovo, P. Franceschini, 1995, European Journal of Pediatrics.

Ullrich-Turner phenotype with unusual manifestation in a patient with mosaicism 45,X/47,XX,+18.

A. Guala, P. Franceschini, D. Franceschini, 1996, American journal of medical genetics.

Lower lip pits and complete idiopathic precocious puberty in a patient with Kabuki make-up (Niikawa-Kuroki) syndrome.

A. Guala, A. Corrias, P. Franceschini, 1993, American journal of medical genetics.

Italian guidelines on the assessment and management of pediatric head injury in the emergency department

R. Manara, N. Parri, A. Amigoni, 2018, Italian Journal of Pediatrics.

Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndrome.

R. Lala, P. Matarazzo, P. Franceschini, 1992, American journal of medical genetics.

The Williams syndrome: an Italian collaborative study.

G. Scarano, O. Gabrielli, G. Neri, 1996, Minerva pediatrica.