Human Chromosome 21 SNP Database

Human Chromosome 21 cSNP. A joint project between the Division of Medical. Of the University of Geneva Medical School. The Swiss Institute of Bioinformatics. Chromosome 21 is the smallest human chromosome, the long arm of which comprises 34 MB of DNA sequence. The completion of its nucleotide sequence revealed 225 genes. It is associated with a number of human pathologies such as Down syndrome, as well as several monogenic and complex genetic disorders. MailtoSamuel.Deutschmedicine.unige.ch.

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TITLE

Human Chromosome 21 SNP Database

DESCRIPTION

Human Chromosome 21 cSNP. A joint project between the Division of Medical. Of the University of Geneva Medical School. The Swiss Institute of Bioinformatics. Chromosome 21 is the smallest human chromosome, the long arm of which comprises 34 MB of DNA sequence. The completion of its nucleotide sequence revealed 225 genes. It is associated with a number of human pathologies such as Down syndrome, as well as several monogenic and complex genetic disorders. MailtoSamuel.Deutschmedicine.unige.ch.

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This web page csnp.isb-sib.ch has the following in the web site, "A joint project between the Division of Medical." Our analyzers viewed that the website also stated " Of the University of Geneva Medical School." The Website also said " The Swiss Institute of Bioinformatics. Chromosome 21 is the smallest human chromosome, the long arm of which comprises 34 MB of DNA sequence. The completion of its nucleotide sequence revealed 225 genes. It is associated with a number of human pathologies such as Down syndrome, as well as several monogenic and complex genetic disorders."

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Human Chromosome 21 SNP Database

A joint project between the Division of Medical. Of the University of Geneva Medical School. The Swiss Institute of Bioinformatics. Chromosome 21 is the smallest human chromosome, the long arm of which comprises 34 MB of DNA sequence. The completion of its nucleotide sequence revealed 225 genes. It is associated with a number of human pathologies such as Down syndrome, as well as several monogenic and complex genetic disorders.

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