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Publications by Cristina Gervasini

Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes

Frontiers in Genetics

Molecular Medicine

English

Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations

Frontiers in Pediatrics

English

Related publications

Molecular Analyses of the BORIS Gene in Children With Silver-Russell Syndrome

International Journal of Human Genetics

English

Molecular Analyses of the BORIS Gene in Children With Silver-Russell Syndrome

International Journal of Human Genetics

English

Myoclonus-Dystonia Syndrome Associated With Russell Silver Syndrome

Movement Disorders

English

Orphan Diseases: Russell - Silver Syndrome

Clinical & experimental pathology

English

Quality of Life in Children With Silver-Russell Syndrome

Pediatric Endocrinology

English

MEF2C-Related 5q14.3 Microdeletion Syndrome Detected by Array CGH: A Case Report

Annals of Rehabilitation Medicine

English

Uncovering Common Pathogenic Transcriptional Dysregulations in Silver-Russell Syndrome

Molecular and Cellular Pediatrics

Molecular Biology

English

Genotype-Phenotype Correlation in 21 Patients With Wolf-Hirschhorn Syndrome Using High Resolution Array Comparative Genome Hybridisation (CGH)

Journal of Medical Genetics

English

Systemic and Maxillofacial Characteristics of 11 Japanese Children With Russell-Silver Syndrome

Congenital Anomalies

Developmental Biology

English