Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 4

1.

Recurrent inversion events at 17q21.31 microdeletion locus are linked to the MAPT H2 haplotype.

Rao PN, Li W, Vissers LE, Veltman JA, Ophoff RA.

Cytogenet Genome Res. 2010;129(4):275-9. doi: 10.1159/000315901.

2.

From 1997 to 2007: a decade journey through the H1 haplotype on 17q21 chromosome.

Kalinderi K, Fidani L, Bostantjopoulou S.

Parkinsonism Relat Disord. 2009 Jan;15(1):2-5. doi: 10.1016/j.parkreldis.2008.03.001. Review.

PMID:
18424220
3.

Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiens.

Hardy J, Pittman A, Myers A, Gwinn-Hardy K, Fung HC, de Silva R, Hutton M, Duckworth J.

Biochem Soc Trans. 2005 Aug;33(Pt 4):582-5. Review.

PMID:
16042549
4.

Novel microdeletion syndromes detected by chromosome microarrays.

Slavotinek AM.

Hum Genet. 2008 Aug;124(1):1-17. doi: 10.1007/s00439-008-0513-9. Review.

PMID:
18512078

Supplemental Content

Support Center