While most variable power optics zoom in on the target but maintain the same zero, 1P21 actually adjusts the BDC based on the zoom.

2009年5月18日 · A hemizygous 1p21 deletion identified by one red (1p21) and two green (1qh) signals was detected by cIg-FISH in 36 (18%) of 203 patients. The median percent of …

2015年3月2日 · Several important neurodevelopmental genes are affected by the 3.56 Mb copy number gain of 1p21.3p21.2, which may be considered reciprocal in gene content to the …

Deletions involving chromosome 1p are frequent events in multiple myeloma (MM). As karyotyping and single nucleotide polymorphism-based mapping analysis identify a minimal …

We describe an as yet unreported neocentric small supernumerary marker chromosome (sSMC) derived from chromosome 1p21.3p21.2. It was present in 80% of the lymphocytes in a male …

目的 探讨新型遗传学指标1p21位点缺失在多发性骨髓瘤(MM)患者中的缺失率、临床相关性和预后意义.方法 以接受沙利度胺为基础治疗的78例初治MM患者为研究对象,以定位于1p21位点的细 …

2007年11月16日 · Our results indicate that del (1p21) is a novel genetic risk factor and warrant inclusion of this genetic aberration in the risk-stratification of MM. Further studies are required …

1p21.3微缺失综合症，也被称为单体型1p21.3。 与1p21.3微缺失综合症相关的重要基因是DPYD（二氢嘧啶脱氢酶）。 相关组织包括眼睛，相关表型为智力障碍和全球发育延迟。

In the present study, we have performed a genome-wide association meta-analysis of TFM adj in 11,569 participants from 6 GWAS samples, and have identified a functional variant …

The combination of fluorescence in situ hybridization with cytoplasmic light chain detection identified chromosome 1p21 deletion in 18 (20%) of 87 patients with multiple myeloma. 1p21 …