A novel interstitial deletion of chromosome 2q21.1‐q23.3: Case report and literature review
Abstract Background Interstitial deletions of 2q are rare. Those that have been reported show varying clinical manifestations according to the size of the deletion and the genomic region involved. Method and Results We describe a preterm male harboring a novel interstitial deletion encompassing the...
Main Authors: | Bader Almuzzaini, Nasser S. Alatwi, Saif Alsaif, Mohammed A. Al Balwi |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2020-04-01
|
Series: | Molecular Genetics & Genomic Medicine |
Subjects: | |
Online Access: | https://doi.org/10.1002/mgg3.1135 |
Similar Items
-
Report of trisomy 2q34-qter and monosomy 4q35.2-qter in a child with mild dysmorphic syndrome and karyotype 46,XY,der(4)t(2;4)(q34;q35.2)pat
by: Juan Pablo Meza-Espinoza, et al.
Published: (2020-05-01) -
7q36 deletion and 9p22 duplication: effects of a double imbalance
by: Pelegrino Karla de, et al.
Published: (2013-01-01) -
Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements
by: Chih-Ping Chen, et al.
Published: (2012-06-01) -
Consequences of 22q11.2 Microdeletion on the Genome, Individual and Population Levels
by: Małgorzata Karbarz
Published: (2020-08-01) -
Cytogenomic characterization of a de novo 4q34.1 deletion in a girl with mild dysmorphic features and a coagulation disorder
by: Juan Pablo Meza-Espinoza, et al.
Published: (2021-09-01)