Twelve X-chromosomal short tandem repeat (STR) markers were typed by means of two multiplex PCR systems. Multiplex I included DXS6789, HumARA, GATA172D05, DXS101, DXS8378, and DXS8377; multiplex II comprised DXS7132, DXS6800, DXS6803, DXS7424, HPRTB, and DXS10011. Allelic frequencies for these loci were determined in a North-West Italian population sample (n = 140; 70 females and 70 males).
Analysis of 12X-chromosomal short tandem repeats in North-West italian population by means of two multiplex PCRs
GINO Sarah;
2006-01-01
Abstract
Twelve X-chromosomal short tandem repeat (STR) markers were typed by means of two multiplex PCR systems. Multiplex I included DXS6789, HumARA, GATA172D05, DXS101, DXS8378, and DXS8377; multiplex II comprised DXS7132, DXS6800, DXS6803, DXS7424, HPRTB, and DXS10011. Allelic frequencies for these loci were determined in a North-West Italian population sample (n = 140; 70 females and 70 males).File in questo prodotto:
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