Cargando…
Genome annotation of a 1.5 Mb region of human chromosome 6q23 encompassing a quantitative trait locus for fetal hemoglobin expression in adults
BACKGROUND: Heterocellular hereditary persistence of fetal hemoglobin (HPFH) is a common multifactorial trait characterized by a modest increase of fetal hemoglobin levels in adults. We previously localized a Quantitative Trait Locus for HPFH in an extensive Asian-Indian kindred to chromosome 6q23....
Autores principales: | Close, James, Game, Laurence, Clark, Barnaby, Bergounioux, Jean, Gerovassili, Ageliki, Thein, Swee Lay |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2004
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC441375/ https://www.ncbi.nlm.nih.gov/pubmed/15169551 http://dx.doi.org/10.1186/1471-2164-5-33 |
Ejemplares similares
-
Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in Tanzania
por: Nkya, Siana, et al.
Publicado: (2017) -
Genome Wide Association Study of Fetal Hemoglobin in Sickle Cell Anemia in Tanzania
por: Mtatiro, Siana Nkya, et al.
Publicado: (2014) -
Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer
por: Mtatiro, Siana N, et al.
Publicado: (2015) -
Relationship between Chlamydia-Ureaplasma-Mycoplasma
Genital Detection with Semen Concentration and
Motility among Greek Men
por: Gerovassili, Ageliki, et al.
Publicado: (2017) -
De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus
por: Tan, Ene-Choo, et al.
Publicado: (2013)