List of works - Marta Unolt

22q and two: 22q11.2 deletion syndrome and coexisting conditions.

scientific article

Aortic arch interruption without ductus arteriosus and no ventricular septal defect.

scientific article published in January 2013

Atrioventricular septal defect prognosis for patients with Down syndrome

scientific article published on 25 August 2012

Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects

scientific article published on 20 December 2019

Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.

scientific article published on 26 July 2017

Congenital heart disease, genetic syndromes, and major noncardiac malformations

scientific article published on 02 October 2012

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.

scientific article published on 16 April 2018

Congenital heart diseases in women

scientific article published in February 2013

Double-orifice left atrioventricular valve in patients with atrioventricular septal defect with and without down syndrome

scientific article published on 01 May 2013

Double-outlet left ventricle with L-malposition of the great arteries and subpulmonary ventricular septal defect.

scientific article

Factors That Negatively Affect the Prognosis of Pediatric Community-Acquired Pneumonia in District Hospital in Tanzania.

scientific article published on 13 March 2017

Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice

scientific article published on 01 April 2019

Myoclonic epilepsy, parkinsonism, schizophrenia and left-handedness as common neuropsychiatric features in 22q11.2 deletion syndrome

scientific article published on 10 September 2019

Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition

scientific article published on 02 September 2019

Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome.

scientific article published on 12 February 2018

Smith-Lemli-Opitz syndrome, cardiac defects, and spleen anomalies

scientific article published on 27 September 2012

Some Isolated Cardiac Malformations Can Be Related to Laterality Defects.

scientific article

Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndrome.

scientific article published on 21 December 2015

Transposition of great arteries: new insights into the pathogenesis

scientific article

Use of a Pediatric Syncope Unit Improves Diagnosis and Lowers Costs: A Hospital-Based Experience

scientific article published on 28 June 2018

What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia

scientific article published in October 2018

List of works by Marta Unolt

22q and two: 22q11.2 deletion syndrome and coexisting conditions.

Aortic arch interruption without ductus arteriosus and no ventricular septal defect.

Atrioventricular septal defect prognosis for patients with Down syndrome

Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects

Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.

Congenital heart disease, genetic syndromes, and major noncardiac malformations

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.

Congenital heart diseases in women

Double-orifice left atrioventricular valve in patients with atrioventricular septal defect with and without down syndrome

Double-outlet left ventricle with L-malposition of the great arteries and subpulmonary ventricular septal defect.

Factors That Negatively Affect the Prognosis of Pediatric Community-Acquired Pneumonia in District Hospital in Tanzania.

Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice

Myoclonic epilepsy, parkinsonism, schizophrenia and left-handedness as common neuropsychiatric features in 22q11.2 deletion syndrome

Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition

Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome.

Smith-Lemli-Opitz syndrome, cardiac defects, and spleen anomalies

Some Isolated Cardiac Malformations Can Be Related to Laterality Defects.

Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndrome.

Transposition of great arteries: new insights into the pathogenesis

Use of a Pediatric Syncope Unit Improves Diagnosis and Lowers Costs: A Hospital-Based Experience

What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia