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Publications by D. Stavropoulos

Microdeletion of 18q21.31 Encompassing the Mc4r Gene Presenting With Obesity and Developmental Delay

Canadian Journal of Diabetes

Internal Medicine

English

Related publications

Microdeletion 9q22.3 Syndrome Includes Metopic Craniosynostosis, Hydrocephalus, Macrosomia, and Developmental Delay

American Journal of Medical Genetics, Part A

English

Facial Dysmorphism-Developmental Delay-Behavioral Abnormalities Syndrome Due to 10p11.21p12.31 Microdeletion

English

A 3.1-Mb Microdeletion of 3p21.31 Associated With Cortical Blindness, Cleft Lip, CNS Abnormalities, and Developmental Delay

European Journal of Medical Genetics

English

A Novel Mc4r Deletion Coexisting With FTO and Mc1r Gene Variants, Causes Severe Early Onset Obesity

English

The Human Mc4r Promoter: Characterization and Role in Obesity

Internal Medicine

English

A Review of the Genomic Analysis of Children Presenting With Developmental Delay/Intellectual Disability and Associated Dysmorphic Features

English

The V103I Polymorphism of the Mc4r Gene and Obesity: Population Based Studies and Meta-Analysis of 29 563 Individuals

International Journal of Obesity

English

A Korean Case of Β-Ureidopropionase Deficiency Presenting With Intractable Seizure, Global Developmental Delay, and Microcephaly

Internal Medicine

Molecular Biology

English

Microdeletion of 6q16.1 Encompassing EPHA7 in a Child With Mild Neurological Abnormalities and Dysmorphic Features: Case Report

Molecular Cytogenetics

Molecular Medicine

Molecular Biology

English