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Publications by Harinder R. Singh
A Novel Alu-Mediated Xq28 Microdeletion Ablates TAZ and Partially Deletes DNL1L in a Patient With Barth Syndrome
American Journal of Medical Genetics, Part A
Genetics
Neonatal Supraventricular Tachycardia (SVT)
NeoReviews
Child Health
Pediatrics
Perinatology
Related publications
A Novel 22q11.2 Microdeletion in DiGeorge Syndrome
American Journal of Human Genetics
Genetics
AAV9-TAZ Gene Replacement Ameliorates Cardiac TMT Proteomic Profiles in a Mouse Model of Barth Syndrome
Molecular Therapy - Methods and Clinical Development
Molecular Medicine
Genetics
Molecular Biology
Interstitial 22q11 Microdeletion Excluding the ADU Breakpoint in a Patient With DiGeorge Syndrome
Human Molecular Genetics
Medicine
Genetics
Molecular Biology
Y Chromosome Microdeletion in a Case With Klinefelter's Syndrome
Archives of Andrology
Alu in Lynch Syndrome: A Danger SINE?
Cancer Prevention Research
Medicine
Cancer Research
Oncology
Medical Genetics: Advances in Brief: Duplication in the Hypoxanthine Phosphoribosyl-Transferase Gene Caused by Alu-Alu Recombination in a Patient With Lesch-Nyhan Syndrome
Journal of Medical Genetics
Genetics
A Drosophila Model of Barth Syndrome
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Distal Xq28 Microduplication Syndrome
RNA Secondary Structure Mediated by Alu Insertion as a Novel Disease-Causing Mechanism
