X-Chromosomal Translocation and Segmental Hypopigmentation — NEJM  hypomelanosis of Ito

X-Chromosomal Translocation and Segmental Hypopigmentation — NEJM hypomelanosis of Ito

Images in Clinical Medicine from The New England Journal of Medicine — X-Chromosomal Translocation and Segmental Hypopigmentation

Images in Clinical Medicine from The New England Journal of Medicine — X-Chromosomal Translocation and Segmental Hypopigmentation

Chromosomal translocation & associated neoplasms...

Chromosomal translocation & associated neoplasms...

The chromosomal translocation characteristic of 70 percent of MCL(Mantel Cell Lymphoma) cases occurs between chromosomes 11 and 14 resulting in the overexpression of cyclinD1

The chromosomal translocation characteristic of 70 percent of MCL(Mantel Cell Lymphoma) cases occurs between chromosomes 11 and 14 resulting in the overexpression of cyclinD1

BCR-ABL1 is a fusion gene formed as a result of the t(9;22)(q34;q11) chromosomal translocation, the translocation that results in the formation of the Philadelphia chromosome. The Abelson murine le...

BCR-ABL1 is a fusion gene formed as a result of the t(9;22)(q34;q11) chromosomal translocation, the translocation that results in the formation of the Philadelphia chromosome. The Abelson murine le...

Ewing/PNET characteristic t(11;22) (q24;q12) leading to EWS-FLI1 fusion is encountered in 85% of Ewing Sarcoma/PNET cases. The majority of remaining cases (10-15%) demonstrate fusion of the EWS gene with a second member of the ETS family of genes, namely ERG. The EWS-ERG fusion occurs as a result of chromosomal translocation t(21;22)(q22;q12)

Ewing/PNET characteristic t(11;22) (q24;q12) leading to EWS-FLI1 fusion is encountered in 85% of Ewing Sarcoma/PNET cases. The majority of remaining cases (10-15%) demonstrate fusion of the EWS gene with a second member of the ETS family of genes, namely ERG. The EWS-ERG fusion occurs as a result of chromosomal translocation t(21;22)(q22;q12)

In genetics, a chromosome translocation is a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes

In genetics, a chromosome translocation is a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes

#NIH scientists visualize how #cancer chromosome abnormalities form in living cells. (Image: A chromosome translocation visualized in 3D) irp.nih.gov

#NIH scientists visualize how #cancer chromosome abnormalities form in living cells. (Image: A chromosome translocation visualized in 3D) irp.nih.gov

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