M. Lecora

Prevalence and Clinical Picture of Celiac Disease in Italian Down Syndrome Patients: A Multicenter Study

O. Gabrielli, A. Giannotti, G. Andria, 2001, Journal of pediatric gastroenterology and nutrition.

T Cell Activation Deficiency Associated with an Aberrant Pattern of Protein Tyrosine Phosphorylation after CD3 Perturbation in Down's Syndrome

C. Pignata, L. Racioppi, G. Matarese, 1998, Pediatric Research.

Phenylketonuria in Italy: Distinct distribution pattern of three mutations of the phenylalanine hydroxylase gene

I. Dianzani, S. Giannattasio, G. Andria, 1997, Journal of Inherited Metabolic Disease.

Clinical and biochemical screening for Smith–Lemli–Opitz syndrome

G. Corso, G. Andria, G. Parenti, 1996 .

Growth retardation, developmental delay, distinctive face, multiple endocrine abnormalities, and adenylyl cyclase dysfunction: A new syndrome?

G. Andria, M. Lecora, M. Salerno, 2003, American Journal of Medical Genetics. Part A.

Geleophysic dysplasia: 7-year follow-up study of a patient with an intermediate form.

G. Andria, L. Titomanlio, G. Parenti, 1999, American journal of medical genetics.

Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients.

M. P. Sperandeo, G. Andria, P. Chiurazzi, 1999, American journal of medical genetics.

Polysyndactyly and trigonocephaly with partial agenesis of corpus callosum.

G. Andria, V. Guzzetta, M. Lecora, 1996, Clinical dysmorphology.

New case of bilateral upper limb amelia, facial clefts, and renal hypoplasia.

G. Andria, I. Scala, M. Lecora, 2000, American journal of medical genetics.

Prenatal ultrasound diagnosis of Roberts syndrome in a family with negative history

M. D'armiento, D. Paladini, P. Martinelli, 1996, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.