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Publications by Holly Mensch

A 22q11.2 Deletion That Excludes UFD1L and CDC45L in a Patient With Conotruncal and Craniofacial Defects

American Journal of Human Genetics

English

Related publications

Acute Dystonia in a Patient With 22q11.2 Deletion Syndrome

English

Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome

American Journal of Human Genetics

English

The Impact of 22q11.2 Deletion Syndrome on Surgical Repair Outcomes of Conotruncal Cardiac Anomalies

Annals of Thoracic Surgery

Respiratory Medicine

Cardiovascular Medicine

English

MPP1/p55 Gene Deletion in a Hemophilia a Patient With Ectrodactyly and Severe Developmental Defects

American Journal of Hematology

English

Schizophrenia and 22q11.2 Deletion Syndrome

Current Psychiatry Reports

English

Hematological Abnormalities and 22q11.2 Deletion Syndrome

Revista Brasileira de Hematologia e Hemoterapia

English

Obesity in Adults With 22q11.2 Deletion Syndrome

Genetics in Medicine

English

COMT and Anxiety and Cognition in Children With Chromosome 22q11.2 Deletion Syndrome

Psychiatry Research

Biological Psychiatry

English

All-Cause Mortality and Survival in Adults With 22q11.2 Deletion Syndrome

Genetics in Medicine

English