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Publications by Serajul Islam
Gonadal Mosaicism of Large Terminal De Novo Duplication and Deletion in Siblings With Variable Intellectual Disability Phenotypes
Molecular genetics & genomic medicine
Genetics
Molecular Biology
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De Novo Truncating Variants in PHF21A Cause Intellectual Disability and Craniofacial Anomalies
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De Novo Variants in WDR37 Are Associated With Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
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De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism
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A De Novo 10.1-Mb 3p25 Terminal Deletion Including SETD5 in a Patient With Ptosis and Psychomotor Retardation
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The Importance of Understanding the Behavioural Phenotypes of Genetic Syndromes Associated With Intellectual Disability
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