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Publications by John M. Graham

IRF2BPL Is Associated With Neurological Phenotypes

American Journal of Human Genetics
Genetics
2018English

Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons

American Journal of Human Genetics
Genetics
2019English

Molecular and Neuroimaging Findings in Pontocerebellar Hypoplasia Type 2 (PCH2): Is Prenatal Diagnosis Possible?

American Journal of Medical Genetics, Part A
Genetics
2010English

Mutation Analysis of UBE3A in Angelman Syndrome Patients

American Journal of Human Genetics
Genetics
1998English

Manitoba Aboriginal Kindred With Original Cerebro-Oculo-Facio-Skeletal Syndrome Has a Mutation in the Cockayne Syndrome Group B (CSB) Gene

American Journal of Human Genetics
Genetics
2000English

Limb Reduction Anomalies and Early in Utero Limb Compression

Journal of Pediatrics
Child HealthPediatricsPerinatology
1980English

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