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Publications by Ursula Martiné
Uncovering Common Pathogenic Transcriptional Dysregulations in Silver-Russell Syndrome
Molecular and Cellular Pediatrics
Child Health
Pediatrics
Perinatology
Molecular Biology
Cell Biology
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Orphan Diseases: Russell - Silver Syndrome
Clinical & experimental pathology
Myoclonus-Dystonia Syndrome Associated With Russell Silver Syndrome
Movement Disorders
Neurology
Quality of Life in Children With Silver-Russell Syndrome
Pediatric Endocrinology
Orthodontic Management of Silver-Russell Syndrome. A Case Report
Open Dentistry Journal
Dentistry
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
Systemic and Maxillofacial Characteristics of 11 Japanese Children With Russell-Silver Syndrome
Congenital Anomalies
Child Health
Pediatrics
Perinatology
Medicine
Developmental Biology
Embryology
Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes
Frontiers in Genetics
Genetics
Molecular Medicine
Silver-Russell Syndrome Due to paternalH19/IGF2hypomethylation in a Twin Girl Born After in Vitro Fertilization
American Journal of Medical Genetics, Part A
Genetics