Importance of conventional cytogenetics in the identification of ins(19;X)(q13.1;p11.2q28) and t(1;11)(q10;p10), both, novel cytogenetic abnormalities in a pediatric AML case-Reference-Cited by-同舟云学术

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Importance of conventional cytogenetics in the identification of ins(19;X)(q13.1;p11.2q28) and t(1;11)(q10;p10), both, novel cytogenetic abnormalities in a pediatric AML case

Published:2021-08 Issue: Volume:256-257 Page:17-20
ISSN:2210-7762
Container-title:Cancer Genetics
language:en
Short-container-title:Cancer Genetics

Author:

Shetty Dhanlaxmi,Mohanty Purvi,Talker Elizabeth,Jain Hemani,Chaubal Kruti,Tembhare Prashant^ORCID,Patkar Nikhil,Subramanian Papagudi^ORCID,Moulik Nirmalya Roy,Dhamne Chetan,Narula Gaurav^ORCID,Banavali Shripad

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference10 articles.

1. WHO classification of tumours of haematopoietic and lymphoid tissues;Swerdlow;Blood,2016

2. Rare cytogenetic abnormalities and alteration of micrornas in acute myeloid leukemia and response to therapy;Shahjahani;Oncol Rev,2015

3. Uncommon cytogenetic abnormalities identifying high-risk acute myeloid leukemia in children;Masetti;Future Oncol,2020

4. An international system for human cytogenomic nomenclature (ISCN);McGowan-Jordan,2016

5. https://mitelmandatabase.isb-cgc.org/case_search (Assessed on 30th Dec 2020)

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