Lista de obras - Marta Unolt - Dominio Público Uruguay

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

artículo científico publicado en 2018

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

artículo científico publicado en 2013

Atrioventricular septal defect prognosis for patients with Down syndrome

artículo científico publicado en 2012

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

artículo científico publicado en 2019

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

artículo científico publicado en 2017

Congenital heart disease, genetic syndromes, and major noncardiac malformations

artículo científico publicado en 2012

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

artículo científico publicado en 2018

Congenital heart diseases in women

artículo científico publicado en 2013

Double Outlet Right Ventricle Versus Aortic Dextroposition: Morphologically Distinct Defects ⬇️

artículo científico publicado el 9 de febrero de 2013

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

artículo científico publicado en 2013

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

artículo científico publicado en 2013

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

artículo científico publicado en 2019

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

artículo científico publicado en 2019

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

artículo científico publicado en 2019

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

artículo científico publicado en 2018

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

artículo científico publicado en 2012

Some Isolated Cardiac Malformations Can Be Related to Laterality Defects.

artículo científico publicado en 2018

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

artículo científico publicado en 2015

Transposition of great arteries: new insights into the pathogenesis

artículo científico publicado en 2013

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

artículo científico publicado en 2018

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

artículo científico publicado en 2018

Lista de obras de 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 Outlet Right Ventricle Versus Aortic Dextroposition: Morphologically Distinct Defects ⬇️

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