| Literature DB >> 21739569 |
A Nicoulaz1, F Rubi, L Lieder, R Wolf, B Goeggel-Simonetti, M Steinlin, R Wiest, H M Bonel, A Schaller, S Gallati, B Conrad.
Abstract
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.Entities:
Mesh:
Year: 2011 PMID: 21739569 DOI: 10.1002/ajmg.a.33210
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802