Literature DB >> 7231523

Major rearrangement in the human beta-globin gene cluster.

R W Jones, J M Old, R J Trent, J B Clegg, D J Weatherall.   

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Year:  1981        PMID: 7231523     DOI: 10.1038/291039a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


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  18 in total

1.  A Chinese G gamma + (A gamma delta beta)zero thalassemia deletion: comparison to other deletions in the human beta-globin gene cluster and sequence analysis of the breakpoints.

Authors:  D L Mager; P S Henthorn; O Smithies
Journal:  Nucleic Acids Res       Date:  1985-09-25       Impact factor: 16.971

2.  Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients.

Authors:  R J Matthews; D S Anson; I R Peake; A L Bloom
Journal:  J Clin Invest       Date:  1987-03       Impact factor: 14.808

3.  Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man.

Authors:  D Tuan; E Feingold; M Newman; S M Weissman; B G Forget
Journal:  Proc Natl Acad Sci U S A       Date:  1983-11       Impact factor: 11.205

Review 4.  Developmental genetics of the human haemoglobins.

Authors:  W G Wood; D J Weatherall
Journal:  Biochem J       Date:  1983-10-01       Impact factor: 3.857

Review 5.  DNA polymorphism and molecular pathology of the human globin gene clusters.

Authors:  S E Antonarakis; H H Kazazian; S H Orkin
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

6.  Restriction mapping of a new deletion responsible for G gamma (delta beta)o thalassemia.

Authors:  R W Jones; J M Old; R J Trent; J B Clegg; D J Weatherall
Journal:  Nucleic Acids Res       Date:  1981-12-21       Impact factor: 16.971

Review 7.  The thalassemias: molecular mechanisms of human genetic disease.

Authors:  R A Spritz; B G Forget
Journal:  Am J Hum Genet       Date:  1983-05       Impact factor: 11.025

8.  [Hereditary anemia: genetic basis, clinical characteristics, diagnosis and treatment. WHO Workgroup].

Authors: 
Journal:  Bull World Health Organ       Date:  1983       Impact factor: 9.408

9.  Type I osteogenesis imperfecta: a nonfunctional allele for pro alpha 1 (I) chains of type I procollagen.

Authors:  G S Barsh; K E David; P H Byers
Journal:  Proc Natl Acad Sci U S A       Date:  1982-06       Impact factor: 11.205

10.  Hereditary anaemias: genetic basis, clinical features, diagnosis, and treatment. WHO working group.

Authors: 
Journal:  Bull World Health Organ       Date:  1982       Impact factor: 9.408

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