Related Experiment Video
Updated: May 7, 2026

Generation of Genomic Deletions in Mammalian Cell Lines via CRISPR/Cas9
Published on: January 3, 2015
3p deletion syndrome
1Department of Human Genetics, Guru Nanak Dev University; and , *39-C, Circular Road; Amritsar, Punjab, India. Correspondence to: Dr Anupam Kaur, Reader, Human Genetics, Guru Nanak Dev University Amritsar, Punjab 143 005, India. anupamkaur@yahoo.co.in.
Abstract:
3p deletion is a rare cytogenetic finding. Here we describe a 3 months old male with congenital malformations. His karyotype revealed 3p deletion 46,XY,del(3)(p25-pter). The child had flexion deformity of wrist and elbow which has never been reported before.
More Related Videos
08:22A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
Published on: December 1, 2017
06:41In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Related Concept Videos
Meiosis I
Nondisjunction
Nondisjunction
Nondisjunction
Karyotyping
Pleiotropy