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Publications by Sara Guzzetti

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

Frontiers in Genetics

Molecular Medicine

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

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

Journal of Medical Genetics

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

Congenital Anomalies

Developmental Biology

English