Significados de human chromosome en inglés

The chromosomal distribution of these classes of repeats are shown for human chromosome 16.

Almost every human chromosome contains thousands of individual genes.

This segment includes the mouse homolog of the Down syndrome critical region of human chromosome 21.

Moreover, the genes encoding these two proteins are adjacent to one another on human chromosome 11.

PCR of human x hamster Radiation Hybrids showed localization of CAGE on the human chromosome Xp22.

Genome wide scans have linked regions of nearly every human chromosome to blood pressure related traits.

Interspecies synteny mapping identifies a quantitative trait locus for bone mineral density on human chromosome Xp22.

These also suggest that human chromosome 8 has an important role in development of prostatic cancer.

The molecular analysis of many genetic diseases requires the isolation of probes for defined human chromosome regions.

Recently we found that another housekeeping gene, NPAT, is located upstream of ATM on human chromosome 11.

A probe containing human sequences for CKMT enabled the provisional assignment of CKMT to human chromosome 15.

Using FISH analysis, the ninjurin gene was localized to human chromosome 9q22.

Chromosomal instability was investigated using fluorescence in situ hybridization to visualize chromosomal rearrangements involving the human chromosome.

The MYOZ gene has six exons and maps to human chromosome 10q22.1-q22.2.

Down syndrome (DS) results from triplication of the whole or distal part of human chromosome 21.

All the insert sequences were present as unidentified exons in the amphiphysin I gene on human chromosome 7.