Agatino Battaglia

Calambrone, Italy

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 21 publications

Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome.

Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome.

Journal: European journal of human genetics : EJHG

Published: December 15, 2010

Commentary: Recognizing syndromes with overlapping features: How difficult is it? Considerations generated by the article on differential diagnosis of Smith-Magenis syndrome by Vieira and colleagues.

Commentary: Recognizing syndromes with overlapping features: How difficult is it? Considerations generated by the article on differential diagnosis of Smith-Magenis syndrome by Vieira and colleagues.

Journal: American journal of medical genetics. Part A

Published: November 29, 2010

Further characterization of the new microdeletion syndrome of 16p11.2-p12.2.

Further characterization of the new microdeletion syndrome of 16p11.2-p12.2.

Journal: American journal of medical genetics. Part A

Published: May 19, 2009

Spectrum of epilepsy and electroencephalogram patterns in Wolf-Hirschhorn syndrome: experience with 87 patients.

Spectrum of epilepsy and electroencephalogram patterns in Wolf-Hirschhorn syndrome: experience with 87 patients.

Journal: Developmental medicine and child neurology

Published: April 22, 2009

Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: experience with 87 patients and recommendations for routine health supervision.

Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: experience with 87 patients and recommendations for routine health supervision.

Journal: American journal of medical genetics. Part C, Seminars in medical genetics

Published: October 22, 2008

Filippi syndrome: further clinical characterization.

Filippi syndrome: further clinical characterization.

Journal: American journal of medical genetics. Part A

Published: June 17, 2008

The inv dup (15) or idic (15) syndrome (Tetrasomy 15q).

The inv dup (15) or idic (15) syndrome (Tetrasomy 15q).

Journal: Orphanet journal of rare diseases

Published: March 20, 2008

Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.

Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.

Journal: Pediatrics

Published: February 05, 2008

On the selection of patients with developmental delay/mental retardation and autism spectrum disorders for genetic studies.

On the selection of patients with developmental delay/mental retardation and autism spectrum disorders for genetic studies.

Journal: American journal of medical genetics. Part A

Published: March 09, 2007

Subtelomeric analysis detects a familial 10p;12p rearrangement in two relatives with a distinct syndrome.

Subtelomeric analysis detects a familial 10p;12p rearrangement in two relatives with a distinct syndrome.

Journal: American journal of medical genetics. Part A

Published: December 14, 2006

The FG syndrome: report of a large Italian series.

The FG syndrome: report of a large Italian series.

Journal: American journal of medical genetics. Part A

Published: May 13, 2006

Etiologic yield of autistic spectrum disorders: a prospective study.

Etiologic yield of autistic spectrum disorders: a prospective study.

Journal: American journal of medical genetics. Part C, Seminars in medical genetics

Published: January 19, 2006

Showing 1-12 of 21

Last Updated: 09/26/2026