Landegent J E, Jansen in de Wal N, Fisser-Groen Y M, Bakker E, van der Ploeg M, Pearson P L
Hum Genet. 1986 Aug;73(4):354-7. doi: 10.1007/BF00279100.
The chromosomal localization of a unique DNA fragment, closely linked to Huntington disease (HD), was assessed in situ by hybridization with 2-acetylaminofluorene (AAF) modified probes. In these experiments, a cosmid cloned genomic fragment (c5.5) was used for hybridization. Here we present evidence that confirms the mapping of the D4S10 locus to the p16 region of chromosome 4 and assigns it to the telomere of the short arm.
通过与2-乙酰氨基芴(AAF)修饰的探针进行原位杂交,评估了与亨廷顿病(HD)紧密连锁的一个独特DNA片段的染色体定位。在这些实验中,使用了一个黏粒克隆的基因组片段(c5.5)进行杂交。在此,我们提供的证据证实了D4S10基因座定位于4号染色体的p16区域,并将其定位在短臂的端粒处。