
Chromosomal translocation - Wikipedia
This includes "balanced" and "unbalanced" translocation, with three main types: "reciprocal", "nonreciprocal" and "Robertsonian" translocation. Reciprocal translocation is a chromosome …
Translocation - National Human Genome Research Institute
3 days ago · A translocation, as related to genetics, occurs when a chromosome breaks and the (typically two) fragmented pieces re-attach to different chromosomes. The detection of …
What Are Translocations? What Disorders Do They Cause? - WebMD
Dec 2, 2024 · A translocation chromosome mutation can be of two types — reciprocal and Robertsonian. In a reciprocal translocation, two different chromosomes have exchanged …
Translocation: MedlinePlus Medical Encyclopedia
Nov 1, 2023 · Translocation means a change in location. It often refers to genetics, when part of a chromosome is transferred to another chromosome. Chromosomes are structures that carry …
What Is a Chromosomal Translocation and How Does It Happen?
Jul 24, 2025 · A chromosomal translocation occurs when a piece from one chromosome breaks off and reattaches to a different chromosome, or when two chromosomes swap pieces. This …
What is a translocation? | MyPathologyReport
A translocation is a specific type of genetic change where a piece of one chromosome breaks off and attaches to another chromosome.
Definition of translocation - NCI Dictionary of Cancer Terms
translocation (TRANZ-loh-KAY-shun) A genetic change in which a piece of one chromosome breaks off and attaches to another chromosome. Sometimes pieces from two different …
TRANSLOCATION Definition & Meaning - Merriam-Webster
The meaning of TRANSLOCATION is the act, process, or an instance of changing location or position.
Translocation: Origin, Types and Effects | Genetics
Intra-chromosomal (internal) translocation or shift: A segment of a chromosome is shifted from its original position to some other position within the same chromosome.
Translocation in Genetics Explained - numberanalytics.com
May 26, 2025 · Translocation is a type of chromosomal abnormality where a segment of a chromosome breaks off and attaches to a different chromosome. This genetic rearrangement …