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Publications by Henry A. Adeola

“Next Generation Sequencing Identifies Mutations in GNPTG Gene as a Cause of Familial Form of Scleroderma-Like Disease”

Pediatric Rheumatology

English

Related publications

Next Generation Sequencing in Synovial Sarcoma Reveals Novel Gene Mutations

English

Diagnosis of Mosaic Mutations in the MEN1 Gene by Next Generation Sequencing.

European Journal of Endocrinology

English

Exome Sequencing Identifies MPL as a Causative Gene in Familial Aplastic Anemia

English

Detection and Quantification of Mosaic Mutations in Disease Genes by Next-Generation Sequencing

Journal of Molecular Diagnostics

Forensic Medicine

Molecular Medicine

English

Targeted Next Generation Sequencing Identifies Two Novel Mutations in SEPN1 in Rigid Spine Muscular Dystrophy 1

English

ACAN Mutations as a Cause of Familial Short Stature

Clinical Pediatric Endocrinology

English

Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome

American Journal of Human Genetics

English

Transcription Factor Mutations as a Cause of Familial Myeloid Neoplasms

Journal of Clinical Investigation

English

Cytosine Deamination Is a Major Cause of Baseline Noise in Next-Generation Sequencing

Molecular Diagnosis and Therapy

Molecular Medicine

English