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Publications by Suneeta Madan-Khetarpal
Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome With Intellectual Disability and Developmental Delay
American Journal of Human Genetics
Genetics
Recurrent Deletions and Reciprocal Duplications of 10q11.21q11.23 Including CHAT and SLC18A3 Are Likely Mediated by Complex Low-Copy Repeats
Human Mutation
Genetics
GRIN1 Mutation Associated With Intellectual Disability Alters NMDA Receptor Trafficking and Function
Journal of Human Genetics
Genetics
Infant Botulism in the Very Young Neonate: A Case Series
AJP Reports
Gynecology
Child Health
Pediatrics
Perinatology
Obstetrics
Expanding the Clinical Phenotype of the 3q29 Microdeletion Syndrome and Characterization of the Reciprocal Microduplication
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
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