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

Frontiers in Genetics - Switzerland
doi 10.3389/fgene.2019.00955
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Frontiers Media SA

Related search

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

International Journal of Human Genetics
Genetics
2009English

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

International Journal of Human Genetics
Genetics
2009English

Myoclonus-Dystonia Syndrome Associated With Russell Silver Syndrome

Movement Disorders
Neurology
2013English

Orphan Diseases: Russell - Silver Syndrome

Clinical & experimental pathology
2019English

Quality of Life in Children With Silver-Russell Syndrome

Pediatric Endocrinology
2013English

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

Annals of Rehabilitation Medicine
Rehabilitation
2015English

Uncovering Common Pathogenic Transcriptional Dysregulations in Silver-Russell Syndrome

Molecular and Cellular Pediatrics
Child HealthPediatricsPerinatologyMolecular BiologyCell Biology
2014English

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

Journal of Medical Genetics
Genetics
2007English

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

Congenital Anomalies
Child HealthPediatricsPerinatologyMedicineDevelopmental BiologyEmbryology
2016English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy