These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
149 related articles for article (PubMed ID: 1520631)
1. A family with haemolytic anaemia and three beta-globins: the deletion in haemoglobin Atlanta-Coventry (beta 75 Leu----Pro, 141 Leu deleted) is not present at the nucleotide level. George PM; Myles T; Williamson D; Higuchi R; Symmans WA; Brennan SO Br J Haematol; 1992 May; 81(1):93-8. PubMed ID: 1520631 [TBL] [Abstract][Full Text] [Related]
2. Beta 141 Leu is not deleted in the unstable haemoglobin Atlanta-Coventry but is replaced by a novel amino acid of mass 129 daltons. Brennan SO; Shaw J; Allen J; George PM Br J Haematol; 1992 May; 81(1):99-103. PubMed ID: 1520632 [TBL] [Abstract][Full Text] [Related]
3. Two de novo mutations in one beta globin chain: hemoglobin Atlanta-Coventry, beta 75 Leu----Pro and beta 141 Leu deleted. Brennan SO; Williamson D; Symmans WA; Carrell RW Hemoglobin; 1986; 10(3):225-37. PubMed ID: 3710819 [TBL] [Abstract][Full Text] [Related]
4. Unstable haemoglobin causing haemolytic anaemia: de novo mutation in Sweden identified by PCR. Landin B; Astrom M J Intern Med; 1993 Mar; 233(3):299-302. PubMed ID: 8450301 [TBL] [Abstract][Full Text] [Related]
5. Haemoglobin Tunis-Bizerte: a new alpha 1 globin 129 Leu-->Pro unstable variant with thalassaemic phenotype. Darbellay R; Mach-Pascual S; Rose K; Graf J; Beris P Br J Haematol; 1995 May; 90(1):71-6. PubMed ID: 7786798 [TBL] [Abstract][Full Text] [Related]
6. Two unstable hemoglobins in one individual: Hb Atlanta (beta 75 Leu leads to Pro) and Hb Coventry (beta 141 Leu deleted). Brennan SO; Williamson D; Symmans WA; Carrell RW Hemoglobin; 1983; 7(4):303-12. PubMed ID: 6618886 [TBL] [Abstract][Full Text] [Related]
14. Haemoglobin Lleida: a new alpha 2-globin variant (12 bp deletion) with mild thalassaemic phenotype. Ayala S; Colomer D; Pujades A; Aymerich M; Vives Corrons JL Br J Haematol; 1996 Sep; 94(4):639-44. PubMed ID: 8826886 [TBL] [Abstract][Full Text] [Related]
15. Compound heterozygosity for two alpha-globin gene defects, Hb Taybe (alpha 1; 38 or 39 minus Thr) and a poly A mutation (alpha 2; AATAAA-->AATAAG), results in a severe hemolytic anemia. Pobedimskaya DD; Molchanova TP; Streichman S; Huisman TH Am J Hematol; 1994 Nov; 47(3):198-202. PubMed ID: 7942784 [TBL] [Abstract][Full Text] [Related]