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Publications by Giovanni Battista Ferrero
Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes
Frontiers in Genetics
Genetics
Molecular Medicine
An Atypical 7q11.23 Deletion in a Normal IQ Williams–Beuren Syndrome Patient
European Journal of Human Genetics
Genetics
Related publications
Molecular Analyses of the BORIS Gene in Children With Silver-Russell Syndrome
International Journal of Human Genetics
Genetics
Molecular Analyses of the BORIS Gene in Children With Silver-Russell Syndrome
International Journal of Human Genetics
Genetics
Myoclonus-Dystonia Syndrome Associated With Russell Silver Syndrome
Movement Disorders
Neurology
Orphan Diseases: Russell - Silver Syndrome
Clinical & experimental pathology
Quality of Life in Children With Silver-Russell Syndrome
Pediatric Endocrinology
MEF2C-Related 5q14.3 Microdeletion Syndrome Detected by Array CGH: A Case Report
Annals of Rehabilitation Medicine
Rehabilitation
Uncovering Common Pathogenic Transcriptional Dysregulations in Silver-Russell Syndrome
Molecular and Cellular Pediatrics
Child Health
Pediatrics
Perinatology
Molecular Biology
Cell Biology
Genotype-Phenotype Correlation in 21 Patients With Wolf-Hirschhorn Syndrome Using High Resolution Array Comparative Genome Hybridisation (CGH)
Journal of Medical Genetics
Genetics
Systemic and Maxillofacial Characteristics of 11 Japanese Children With Russell-Silver Syndrome
Congenital Anomalies
Child Health
Pediatrics
Perinatology
Medicine
Developmental Biology
Embryology