Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects.

We have examined the phenotypic effects of 21 independent deletions from the fully sequenced and annotated 356 kb telomeric region of the short arm of chromosome 16 (16p13.3). Fifteen genes contained within this region have been highly conserved throughout evolution and encode proteins involved in i...

Täydet tiedot

Bibliografiset tiedot
Päätekijät: Horsley, S, Daniels, R, Anguita, E, Raynham, H, Peden, J, Villegas, A, Vickers, M, Green, S, Waye, J, Chui, D, Ayyub, H, MacCarthy, AB, Buckle, V, Gibbons, R, Kearney, L, Higgs, D
Aineistotyyppi: Journal article
Kieli:English
Julkaistu: 2001

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