Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers.

Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers.

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http://www.wikidata.org/entity/Q35889124
Genome annotation of a 1.5 Mb region of human chromosome 6q23 encompassing a quantitative trait locus for fetal hemoglobin expression in adultsGlobal genetic architecture of an erythroid quantitative trait locus, HMIP-2Experimental generation of SNP haplotype signatures in patients with sickle cell anaemiaSickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.FOETAL HAEMOGLOBIN (HbF) STATUS IN ADULT SICKLE CELL ANAEMIA PATIENTS IN IBADAN, NIGERIAHaplotype mapping of a major quantitative-trait locus for fetal hemoglobin production, on chromosome 6q23.Linkage analysis in a large Brazilian family with van der Woude syndrome suggests the existence of a susceptibility locus for cleft palate at 17p11.2-11.1.Transcriptional regulation of fetal to adult hemoglobin switching: new therapeutic opportunities.Segregation and linkage analysis of serum angiotensin I-converting enzyme levels: evidence for two quantitative-trait loci.Identification of new polymorphisms of the angiotensin I-converting enzyme (ACE) gene, and study of their relationship to plasma ACE levels by two-QTL segregation-linkage analysis.A genome-wide search replicates evidence of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE) unlinked to the ACE gene.Evidence of genetic interaction between the beta-globin complex and chromosome 8q in the expression of fetal hemoglobin.Control of fetal hemoglobin: new insights emerging from genomics and clinical implications.Hemoglobin switching in humans is accompanied by changes in the ratio of the transcription factors, GATA-1 and SP1.Detection of non-deletional type of hereditary persistence of fetal hemoglobin (HPFH) condition associated with 619 bp β(°)-thalassemia deletion.Recent advances in β-thalassemiasReply to Sham et al.
P2860

Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers.

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http://www.wikidata.org/entity/Q35889124
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1994 nî lūn-bûn
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1994年の論文
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1994年論文
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1994年論文
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1994年論文
@zh-hk
1994年論文
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1994年論文
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1994年论文
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1994年论文
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1994年论文
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name
Detection of a major gene for ...... ounting for genetic modifiers.
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Detection of a major gene for ...... ounting for genetic modifiers.
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type
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Detection of a major gene for ...... ounting for genetic modifiers.
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Detection of a major gene for ...... ounting for genetic modifiers.
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Detection of a major gene for ...... ounting for genetic modifiers.
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Detection of a major gene for ...... ounting for genetic modifiers.
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Detection of a major gene for ...... counting for genetic modifiers
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P2093
P2860
P304
P31
P407
P433
P478
P50
P577
P698
P921
P932