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Annales De Genetique|June 1, 1975
A family with three sibs carrying trisomy 21F Nuzzo, M Stefanini, G Simoni, et al.American Journal of Medical Genetics|November 20, 1995
Short rib-dysplasia group (with/without polydactyly): report of a patient suggesting the existence of a continuous spectrumP Franceschini, A Guala, M P Vardeu, et al.Pediatric Radiology|January 1, 1986
The Coffin-Siris syndrome in two siblingsP Franceschini, M Cirillo Silengo, R Bianco, et al.Minerva Pediatrica|January 1, 1989
[Serum prealbumin standards in the neonatal period]C Fabris, D Licata, E Bertino, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1986
[Surveillance of congenital malformations. Monitoring of polydactyly using the Chen method]C Fabris, D Licata, E Garzena, et al.American Journal of Medical Genetics|December 1, 1992
Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndromeP Franceschini, M P Vardeu, L Dalforno, et al.American Journal of Medical Genetics|September 1, 1993
Lower lip pits and complete idiopathic precocious puberty in a patient with Kabuki make-up (Niikawa-Kuroki) syndromeP Franceschini, M P Vardeu, A Guala, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|January 1, 1996
Fetal growth velocity: kinetic, clinical, and biological aspectsE Bertino, E Di Battista, A Bossi, et al.Journal of Clinical Pathology|April 1, 1993
Intensity of inflammatory damage and serum lipid peroxide concentrations in liver diseaseC Fabris, M Pirisi, M P Panozzo, et al.Journal of Chemotherapy (Florence, Italy)|April 17, 2008
New diagnostic tools for neonatal sepsis: the role of a real-time polymerase chain reaction for the early detection and identification of bacterial and fungal species in blood samplesM Mussap, M P Molinari, E Senno, et al.Pageof 32