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Publications by Robin D. Clark
Microdeletion 9q22.3 Syndrome Includes Metopic Craniosynostosis, Hydrocephalus, Macrosomia, and Developmental Delay
American Journal of Medical Genetics, Part A
Genetics
Rare Missense and Synonymous Variants in UBE1 Are Associated With X-Linked Infantile Spinal Muscular Atrophy
American Journal of Human Genetics
Genetics
Related publications
Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome
Facial Dysmorphism-Developmental Delay-Behavioral Abnormalities Syndrome Due to 10p11.21p12.31 Microdeletion
Microdeletion of 18q21.31 Encompassing the Mc4r Gene Presenting With Obesity and Developmental Delay
Canadian Journal of Diabetes
Internal Medicine
Endocrinology
Metabolism
Medicine
Diabetes
Ossification Anomalies-Psychomotor Developmental Delay Syndrome
3q29 Microdeletion Syndrome
3q13 Microdeletion Syndrome
8q22.1 Microdeletion Syndrome
16q24.3 Microdeletion Syndrome
Spastic Paraplegia-Severe Developmental Delay-Epilepsy Syndrome
