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289 results

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Page 1
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach.
Giardine B, Borg J, Higgs DR, Peterson KR, Philipsen S, Maglott D, Singleton BK, Anstee DJ, Basak AN, Clark B, Costa FC, Faustino P, Fedosyuk H, Felice AE, Francina A, Galanello R, Gallivan MV, Georgitsi M, Gibbons RJ, Giordano PC, Harteveld CL, Hoyer JD, Jarvis M, Joly P, Kanavakis E, Kollia P, Menzel S, Miller W, Moradkhani K, Old J, Papachatzopoulou A, Papadakis MN, Papadopoulos P, Pavlovic S, Perseu L, Radmilovic M, Riemer C, Satta S, Schrijver I, Stojiljkovic M, Thein SL, Traeger-Synodinos J, Tully R, Wada T, Waye JS, Wiemann C, Zukic B, Chui DH, Wajcman H, Hardison RC, Patrinos GP. Giardine B, et al. Among authors: old j. Nat Genet. 2011 Mar 20;43(4):295-301. doi: 10.1038/ng.785. Nat Genet. 2011. PMID: 21423179 Free PMC article.
EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.
Traeger-Synodinos J, Harteveld CL, Old JM, Petrou M, Galanello R, Giordano P, Angastioniotis M, De la Salle B, Henderson S, May A; EMQN haemoglobinopathies best practice meeting. Traeger-Synodinos J, et al. Among authors: old jm. Eur J Hum Genet. 2015 Apr;23(4):426-37. doi: 10.1038/ejhg.2014.131. Epub 2014 Jul 23. Eur J Hum Genet. 2015. PMID: 25052315 Free PMC article.
An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project.
Lederer CW, Basak AN, Aydinok Y, Christou S, El-Beshlawy A, Eleftheriou A, Fattoum S, Felice AE, Fibach E, Galanello R, Gambari R, Gavrila L, Giordano PC, Grosveld F, Hassapopoulou H, Hladka E, Kanavakis E, Locatelli F, Old J, Patrinos GP, Romeo G, Taher A, Traeger-Synodinos J, Vassiliou P, Villegas A, Voskaridou E, Wajcman H, Zafeiropoulos A, Kleanthous M. Lederer CW, et al. Among authors: old j. Hemoglobin. 2009;33(3):163-76. doi: 10.1080/03630260903089177. Hemoglobin. 2009. PMID: 19657830
Direct detection of haemoglobin E with MnlI.
Thein SL, Lynch JR, Old JM, Weatherall DJ. Thein SL, et al. Among authors: old jm. J Med Genet. 1987 Feb;24(2):110-1. doi: 10.1136/jmg.24.2.110. J Med Genet. 1987. PMID: 3031297 Free PMC article. No abstract available.
A novel alpha-globin gene arrangement in man.
Higgs DR, Old JM, Pressley L, Clegg JB, Weatherall DJ. Higgs DR, et al. Among authors: old jm. Nature. 1980 Apr 17;284(5757):632-5. doi: 10.1038/284632a0. Nature. 1980. PMID: 6245373
EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.
Traeger-Synodinos J, Harteveld CL, Old JM, Petrou M, Galanello R, Giordano P, Angastioniotis M, De la Salle B, Henderson S, May A. Traeger-Synodinos J, et al. Among authors: old jm. Eur J Hum Genet. 2015 Apr;23(4):560. doi: 10.1038/ejhg.2015.39. Eur J Hum Genet. 2015. PMID: 25762031 Free PMC article. No abstract available.
Prenatal diagnosis of the common haemoglobin disorders.
Weatherall DJ, Old JM, Thein SL, Wainscoat JS, Clegg JB. Weatherall DJ, et al. Among authors: old jm. J Med Genet. 1985 Dec;22(6):422-30. doi: 10.1136/jmg.22.6.422. J Med Genet. 1985. PMID: 3001310 Free PMC article. Review.
289 results