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The sequence of human chromosome 21 and implications for research into Down syndrome
The recent completion of the DNA sequence of human chromosome 21 has provided the first look at the 225 genes that are candidates for involvement in Down syndrome (trisomy 21). A broad functional classification of these genes, their expression data and evolutionary conservation, and comparison with...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138845/ https://www.ncbi.nlm.nih.gov/pubmed/11178230 |
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author | Gardiner, Katheleen Davisson, Muriel |
author_facet | Gardiner, Katheleen Davisson, Muriel |
author_sort | Gardiner, Katheleen |
collection | PubMed |
description | The recent completion of the DNA sequence of human chromosome 21 has provided the first look at the 225 genes that are candidates for involvement in Down syndrome (trisomy 21). A broad functional classification of these genes, their expression data and evolutionary conservation, and comparison with the gene content of the major mouse models of Down syndrome, suggest how the chromosome sequence may help in understanding the complex Down syndrome phenotype. |
format | Text |
id | pubmed-138845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-1388452003-03-03 The sequence of human chromosome 21 and implications for research into Down syndrome Gardiner, Katheleen Davisson, Muriel Genome Biol Review The recent completion of the DNA sequence of human chromosome 21 has provided the first look at the 225 genes that are candidates for involvement in Down syndrome (trisomy 21). A broad functional classification of these genes, their expression data and evolutionary conservation, and comparison with the gene content of the major mouse models of Down syndrome, suggest how the chromosome sequence may help in understanding the complex Down syndrome phenotype. BioMed Central 2000 2000-08-04 /pmc/articles/PMC138845/ /pubmed/11178230 Text en Copyright © 2000 GenomeBiology.com |
spellingShingle | Review Gardiner, Katheleen Davisson, Muriel The sequence of human chromosome 21 and implications for research into Down syndrome |
title | The sequence of human chromosome 21 and implications for research into Down syndrome |
title_full | The sequence of human chromosome 21 and implications for research into Down syndrome |
title_fullStr | The sequence of human chromosome 21 and implications for research into Down syndrome |
title_full_unstemmed | The sequence of human chromosome 21 and implications for research into Down syndrome |
title_short | The sequence of human chromosome 21 and implications for research into Down syndrome |
title_sort | sequence of human chromosome 21 and implications for research into down syndrome |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138845/ https://www.ncbi.nlm.nih.gov/pubmed/11178230 |
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