Division of Human Genetics, Bern University Children's Hospital, Bern, Switzerland.
Am J Med Genet A. 2011 Aug;155A(8):1964-8. doi: 10.1002/ajmg.a.33210. Epub 2011 Jul 7.
Monosomy 1p36 results from heterozygous deletions of the terminal short chromosome 1 arm, the most common terminal deletion in humans. The microdeletion is split in two usually non-overlapping and clinically distinct classical distal and proximal 1p36 monosomy syndromes. Using comparative genome hybridization, MLPA and qPCR we identified the largest contiguous ∼16 Mb terminal 1p36 deletion reported to date. It covers both distal and proximal regions, causes a neonatally lethal variant with virtually exclusive features of distal 1p36 monosomy, highlighting the key importance of the gene-rich distal region for the "compound" 1p36 phenotype and a threshold deletion-size effect for haplo-lethality.
单体性 1p36 是由于短臂 1 号染色体末端的杂合性缺失所致,这是人类中最常见的末端缺失。微缺失通常分为不重叠且临床特征明显不同的经典远端和近端 1p36 单体性综合征。使用比较基因组杂交、MLPA 和 qPCR,我们鉴定出了迄今为止报道的最大的连续约 16Mb 末端 1p36 缺失。它覆盖了远端和近端区域,导致了一种新生儿致死性变体,几乎只具有远端 1p36 单体性的特征,突出了基因丰富的远端区域对“复合”1p36 表型的关键重要性以及单倍体致死性的缺失大小效应阈值。