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Publications by Kairit Joost
The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver–Russell Syndrome and Beckwith–Wiedemann Syndrome
Genetic Testing and Molecular Biomarkers
Medicine
Genetics
Related publications
Beckwith-Wiedemann Syndrome
Evidence for Anticipation in Beckwith–Wiedemann Syndrome
European Journal of Human Genetics
Genetics
The Two-Domain Hypothesis in Beckwith-Wiedemann Syndrome
Journal of Clinical Investigation
Medicine
Molecular Diagnosis of Beckwith-Wiedemann Syndrome Using Quantitative Methylation-Sensitive Polymerase Chain Reaction
Genetics in Medicine
Medicine
Genetics
Obstructive Sleep Apnea in Children With Beckwith-Wiedemann Syndrome
Journal of Clinical Sleep Medicine
Pulmonary
Neurology
Respiratory Medicine
Kagami‐Ogata Syndrome: An Important Differential Diagnosis to Beckwith‐Wiedemann Syndrome
Journal of Clinical Ultrasound
Nuclear Medicine
Radiology
Imaging
Paradoxical NSD1 Mutations in Beckwith-Wiedemann Syndrome and 11p15 Anomalies in Sotos Syndrome
American Journal of Human Genetics
Genetics
Orphan Diseases: Russell - Silver Syndrome
Clinical & experimental pathology
Adrenocortical Adenoma in a Sudanese Girl With Beckwith-Wiedemann Syndrome
International Journal of Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
