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Publications by S. MERGENTHALER
Exclusion of a Disease Relevant Role of PAX4 in the Aetiology of Silver-Russell Syndrome: Screening for Mutations and Determination of Imprinting Status
Journal of Medical Genetics
Genetics
Related publications
Orthodontic Management of Silver-Russell Syndrome. A Case Report
Open Dentistry Journal
Dentistry
Orphan Diseases: Russell - Silver Syndrome
Clinical & experimental pathology
Quality of Life in Children With Silver-Russell Syndrome
Pediatric Endocrinology
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
Molecular Analyses of the BORIS Gene in Children With Silver-Russell Syndrome
International Journal of Human Genetics
Genetics
Maternal Repression of the Human GRB10 Gene in the Developing Central Nervous System; Evaluation of the Role for GRB10 in Silver-Russell Syndrome
European 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
Trisomy 7 Mosaicism, Maternal Uniparental Heterodisomy 7 and Hirschsprung's Disease in a Child With Silver–Russell Syndrome
European Journal of Human Genetics
Genetics
