Pages that link to "Q28282726"

The following pages link to Partial deletion of the alpha-globin structural gene in human alpha-thalassaemia (Q28282726):

Displaying 34 items.

• The molecular basis of alpha-thalassaemia in Thailand (Q33939759) (← links)
• The molecular genetics of human hemoglobin (Q34258836) (← links)
• Alternative splicing of human elastin mRNA indicated by sequence analysis of cloned genomic and complementary DNA. (Q34338142) (← links)
• The thalassemias: molecular mechanisms of human genetic disease. (Q35202896) (← links)
• Mutation in an intervening sequence splice junction in man (Q35464330) (← links)
• Three mouse models of human thalassemia (Q35464805) (← links)
• An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotype (Q35581948) (← links)
• A new type of illegitimate recombination is dependent on restriction and homologous interaction. (Q35628949) (← links)
• Compilation of DNA strand exchange sites for non-homologous recombination in somatic cells (Q36054067) (← links)
• A large deletion encompassing the entire alpha-like globin gene cluster in a family of northern European extraction (Q36077209) (← links)
• Genetic and molecular diversity in nondeletion Hb H disease (Q36370539) (← links)
• Deletions in the alpha-globin gene complex in alpha-thalassemic mice (Q36383841) (← links)
• Structure of the 3' region of the human elastin gene: great abundance of Alu repetitive sequences and few coding sequences (Q36427166) (← links)
• Heterogeneity of DNA deletion in gamma delta beta-thalassemia (Q36996879) (← links)
• Molecular basis for HbH disease in Italy: geographical distribution of deletional and nondeletional alpha-thalassemia haplotypes (Q38972232) (← links)
• DNA polymorphism and molecular pathology of the human globin gene clusters (Q39813814) (← links)
• The Molecular Genetics of Thalassemia (Q40125860) (← links)
• Characterisation of a new α thalassemia 1 defect due to a partial deletion of the α globin gene complex (Q40482451) (← links)
• Human alpha-thalassemia syndromes: detection of molecular defects (Q41189224) (← links)
• A mutational hot-spot within an intron of the mouse beta 2-microglobulin gene (Q42095940) (← links)
• Phenotype-genotype correlation in haemoglobin H disease in childhood. (Q42654122) (← links)
• Molecular pathology of alpha-thalassemia (Q43997935) (← links)
• Prenatal diagnosis of alpha-thalassemia by polymerase chain reaction and dual restriction enzyme analysis (Q44122144) (← links)
• Human alpha-globin gene expression is silenced by terminal truncation of chromosome 16p beginning immediately 3' of the zeta-globin gene (Q45161254) (← links)
• A gene deletion ending at the midpoint of a repetitive DNA sequence in one form of hereditary persistence of fetal haemoglobin (Q46527819) (← links)
• Evolution of Alu family repeats since the divergence of human and chimpanzee (Q48383406) (← links)
• Structural analysis of templates and RNA polymerase III transcripts of Alu family sequences interspersed among the human β-like globin genes (Q48410538) (← links)
• ?-Globin gene deletion causes ?-thalassemia syndromes in two German families (Q53817315) (← links)
• (Q56603065) (redirect page) (← links)
• The levels of zeta, gamma, and delta chains in patients with Hb H disease (Q69370069) (← links)
• A mutant lymphoma cell line with a defective Thy-1 glycoprotein gene (Q69894328) (← links)
• Heterogeneity of the alpha-globin gene defects in German alpha-thalassemia affected families (Q70101104) (← links)
• Frequent occurrence of a ζ-globin-region deletion in american blacks accounts for a previously-described restriction site polymorphism (Q72408016) (← links)
• The molecular and hematological heterogeneity of alpha thalassemia (Q72412710) (← links)