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Publications by Z. Mohammed

Familial Russell–Silver Syndrome Like Phenotype in the PCNA Domain of the CDKN1C Gene, a Further Case

Case Reports in Genetics

English

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Hypomethylation of the H19 Gene Causes Not Only Silver-Russell Syndrome (SRS) but Also Isolated Asymmetry or an SRS-Like Phenotype

American Journal of Human Genetics

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Orthodontic Management of Silver-Russell Syndrome. A Case Report

Open Dentistry Journal

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

International Journal of Human Genetics

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

International Journal of Human Genetics

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Orphan Diseases: Russell - Silver Syndrome

Clinical & experimental pathology

English

Myoclonus-Dystonia Syndrome Associated With Russell Silver Syndrome

Movement Disorders

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Quality of Life in Children With Silver-Russell Syndrome

Pediatric Endocrinology

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Uncovering Common Pathogenic Transcriptional Dysregulations in Silver-Russell Syndrome

Molecular and Cellular Pediatrics

Molecular Biology

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Bartter Syndrome-Like Phenotype in a Patient With Diabetes: A Case Report

Journal of Medical Case Reports

English