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Publications by V Fraser
A Family Study of Craniosynostosis, With Probable Recognition of a Distinct Syndrome.
Journal of Medical Genetics
Genetics
Related publications
Family Study of Inherited Syndrome With Multiple Congenital Deformities: Symphalangism, Carpal and Tarsal Fusion, Brachydactyly, Craniosynostosis, Strabismus, Hip Osteochondritis.
Journal of Medical Genetics
Genetics
Bloom's Syndrome: A Probable New Case With Cytogenetic Findings.
Journal of Medical Genetics
Genetics
Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome
537 Hypophosphatasia (A Family Study) and Turner Syndrome
Pediatric Research
Child Health
Pediatrics
Perinatology
Familial Aggregation of Irritable Bowel Syndrome: A Family Case–Control Study
American Journal of Gastroenterology
Hepatology
Gastroenterology
ThePtch1DLmouse: A New Model to Study Lambd Craniosynostosis and Basal Cell Nevus Syndrome-Associated Skeletal Defects
Genesis
Medicine
Endocrinology
Genetics
Cell Biology
Distinct Clinical Picture of Cushing’s Syndrome in a Patient With Morris’ Syndrome — First Literature Report
Endokrynologia Polska
Endocrinology
Metabolism
Diabetes
Teaching Family Medicine Approach in Paediatrics With a Patient Having Genetic Syndrome – A Case Study
The Asia Pacific Scholar
Epilepsy in Muenke Syndrome: FGFR3-Related Craniosynostosis
Pediatric Neurology
Child Health
Developmental Neuroscience
Pediatrics
Perinatology
Neurology
