Translocation of an erythroid-specific hypersensitive site in deletion-type hereditary persistence of fetal hemoglobin.

Hereditary persistence of fetal hemoglobin (HPFH) can involve large deletions which eliminate the 3' end of the beta-like globin gene cluster and more than 70 kilobases (kb) of flanking DNA. Blot hybridization revealed a DNase I-hypersensitive site extending from 1.1 to 1.4 kb downstream of the...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Elder, J T, Forrester, W C, Thompson, C, Mager, D, Henthorn, P, Peretz, M, Papayannopoulou, T, Groudine, M
Fformat: Erthygl
Iaith:en
Cyhoeddwyd: 1990
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC362240/
https://ncbi.nlm.nih.gov/pubmed/1690839
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Rhyngrwyd

https://ncbi.nlm.nih.gov/pmc/articles/PMC362240/
https://ncbi.nlm.nih.gov/pubmed/1690839

Eitemau Tebyg