G. Camera

发表

A new patient with Lowry–Wood syndrome with mild phenotype

N. Brunetti‐Pierri, G. Andria, S. Ikegawa, 2003, American journal of medical genetics. Part A.

Congenital hypertrichosis, cardiomegaly, and osteochondrodysplasia (Cantú syndrome): a new case with unusual radiological findings.

P. Strisciuglio, D. Concolino, S. Formicola, 2000, American journal of medical genetics.

Birth prevalence of skeletal dysplasias in the Italian Multicentric Monitoring System for Birth Defects.

P. Mastroiacovo, G. Camera, 1982, Progress in clinical and biological research.

Hydrocephalus, skeletal anomalies, and mental disturbances in a mother and three daughters: a new syndrome.

E. Calzolari, A. Ferlini, P. Gobbi, 1995, American journal of medical genetics.

New multisystemic disorder involving heart valves, skin, bones, and joints in two brothers.

M. Di Rocco, F. Crovato, C. Borrone, 1993, American journal of medical genetics.

Birth prevalence and mutation rate of achondroplasia in the Italian Multicentre Monitoring System for Birth Defects.

P. Mastroiacovo, G. Camera, 1988, Basic life sciences.

An unusual radiological finding in thanatophoric dysplasia type 1 with common mutation of the fibroblast growth factor receptor-3 (FGFR3) gene (Arg248Cys)

M. Baldi, G. Camera, M. Baffico, 1997, American journal of medical genetics.

Occurrence of thanatophoric dysplasia type I (R248C) and hypochondroplasia (N540K) mutations in two patients with achondroplasia phenotype.

P. Mastroiacovo, D. Concolino, G. Camera, 2001, American journal of medical genetics.

Diprosopus with associated malformations: report of two cases.

L. Pavone, M. Barberis, S. Grasso, 1987, American journal of medical genetics.

Sponastrime dysplasia: report on two siblings with metal retardation.

M. Di Rocco, A. Camera, R. Gatti, 1993, Pediatric Radiology.

"C" trigonocephaly syndrome: two additional cases.

A. Selicorni, G. Serra, G. Camera, 1990, American journal of medical genetics.

"Snail-like pelvis" chondrodysplasia: a further case report.

G. Scarano, P. Mastroiacovo, G. La Cava, 1991, American journal of medical genetics.

Congenital hypertrichosis, cardiomegaly, and osteochondrodysplasia (Cantú syndrome): a new case with unusual radiological findings.

P. Strisciuglio, D. Concolino, S. Formicola, 2000, American journal of medical genetics.