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Publications by Ankita Patel
Erratum To: Haploinsufficiency of the E3 Ubiquitin-Protein Ligase Gene TRIP12 Causes Intellectual Disability With or Without Autism Spectrum Disorders, Speech Delay, and Dysmorphic Features
Human Genetics
Genetics
Human Subtelomeric Copy Number Gains Suggest a DNA Replication Mechanism for Formation: Beyond Breakage–fusion–bridge for Telomere Stabilization
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
Neurodevelopmental and Neurobehavioral Characteristics in Males and Females With CDKL5 Duplications
European Journal of Human Genetics
Genetics
Triploidy Mosaicism (45,x/68,xx) in an Infant Presenting With Failure to Thrive
American Journal of Medical Genetics, Part A
Genetics
OEIS Complex Associated With Chromosome 1p36 Deletion: A Case Report and Review
American Journal of Medical Genetics, Part A
Genetics
Transdermal Drug Delivery Systems: A Mini Review.
International Journal of Advanced Research
A Small Recurrent Deletion Within 15q13.3 Is Associated With a Range of Neurodevelopmental Phenotypes
Nature Genetics
Genetics
Variability in Interpreting and Reporting Copy Number Changes Detected by Array-Based Technology in Clinical Laboratories
Genetics in Medicine
Medicine
Genetics
Microduplications of 22q11.2 Are Frequently Inherited and Are Associated With Variable Phenotypes
Genetics in Medicine
Medicine
Genetics
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