File:Three chromosomal abnormalities with ISCN nomenclature.png
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Summary
| Description |
English: Three chromosomal abnormalities with ISCN nomenclature, with increasing complexity: (A) A tumour karyotype in a male with loss of the Y chromosome, (B) Prader–Willi Syndrome i.e. deletion in the 15q11-q12 region and (C) an arbitrary karyotype that involves a variety of autosomal and allosomal abnormalities. |
| Date | |
| Source |
Warrender JD, Moorman AV, Lord P (2019). "A fully computational and reasonable representation for karyotypes.". Bioinformatics 35 (24): 5264-5270. DOI:10.1093/bioinformatics/btz440. PMID 31228194. PMC: 6954653. - "This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/)" |
| Author | Warrender JD, Moorman AV, Lord P |
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 22:26, 27 October 2022 | | 916 × 519 (190 KB) | wikimediacommons>Mikael Häggström | Uploaded a work by Warrender JD, Moorman AV, Lord P from {{cite journal| author=Warrender JD, Moorman AV, Lord P| title=A fully computational and reasonable representation for karyotypes. | journal=Bioinformatics | year= 2019 | volume= 35 | issue= 24 | pages= 5264-5270 | pmid=31228194 | doi=10.1093/bioinformatics/btz440 | pmc=6954653 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=31228194 }}<br>- "This is an Open A... |
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