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Publications by Raihan K Uddin

Breakpoint Associated With a Novel 2.3 Mb Deletion in the VCFS Region of 22q11 and the Role of Alu (SINE) in Recurring Microdeletions

BMC Medical Genetics

English

Related publications

Chromosome 22q11 Microdeletions in Tetralogy of Fallot.

Archives of Disease in Childhood

English

Infertility in a Man With Oligoasthenozoospermia Associated With Mosaic Chromosome 22q11 Deletion

Molecular genetics & genomic medicine

Molecular Biology

English

Interstitial 22q11 Microdeletion Excluding the ADU Breakpoint in a Patient With DiGeorge Syndrome

Human Molecular Genetics

Molecular Biology

English

Alu in Lynch Syndrome: A Danger SINE?

Cancer Prevention Research

Cancer Research

English

Lower Prepulse Inhibition in Children With the 22q11 Deletion Syndrome

American Journal of Psychiatry

English

Movement Disorders in Adults With 22q11 Deletion Syndrome

Movement Disorders Clinical Practice

English

Hereditary Hemorrhagic Telangiectasia: Breakpoint Characterization of a Novel Large Deletion inACVRL1Suggests the Causing Mechanism

Molecular Syndromology

English

A Novel Protein Isoform of the Multicopy Human NAIP Gene Derives From Intragenic Alu SINE Promoters

Multidisciplinary

English

Deletion of 22q11 Chromosome Is Associated With Postoperative Morbidity After Unifocalisation Surgery – CORRIGENDUM

Cardiology in the Young

Cardiovascular Medicine

English