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Journal Abstract Search

148 related items for PubMed ID: 1770527

  • 1.
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  • 2. The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkage.
    Donnai D, Clayton-Smith J, Gibbons RJ, Higgs DR.
    J Med Genet; 1991 Nov; 28(11):742-5. PubMed ID: 1770530
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  • 3. Alpha thalassaemia/mental retardation syndrome (non-deletional type): report of a family supporting X linked inheritance.
    Cole TR, May A, Hughes HE.
    J Med Genet; 1991 Nov; 28(11):734-7. PubMed ID: 1770528
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  • 5. X linked alpha thalassaemia/mental retardation (ATR-X) syndrome.
    Chudley AE, Lowry RB.
    J Med Genet; 1992 May; 29(5):357. PubMed ID: 1583667
    [No Abstract] [Full Text] [Related]

  • 6. The non-deletion type of alpha thalassaemia/mental retardation: a recognisable dysmorphic syndrome with X linked inheritance.
    Wilkie AO, Pembrey ME, Gibbons RJ, Higgs DR, Porteous ME, Burn J, Winter RM.
    J Med Genet; 1991 Oct; 28(10):724. PubMed ID: 1941971
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  • 7. Occurrence of the alpha thalassaemia-mental retardation syndrome (non-deletional type) in an Australian male.
    Harvey MP, Kearney A, Smith A, Trent RJ.
    J Med Genet; 1990 Sep; 27(9):577-81. PubMed ID: 2231651
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  • 8. Genotypes of alpha-thalassemia in the Chinese.
    Huang YW, Wang RX, Zhang NJ, Yang XY, Guo XZ, Li CQ, Zhang J, Liang X, Zhang JW, Wu GY.
    Birth Defects Orig Artic Ser; 1987 Sep; 23(5A):31-8. PubMed ID: 3689913
    [No Abstract] [Full Text] [Related]

  • 9. Alpha thalassaemia mental retardation (ATR-X): an atypical family.
    Logie LJ, Gibbons RJ, Higgs DR, Brown JK, Porteous ME.
    Arch Dis Child; 1994 May; 70(5):439-40. PubMed ID: 8017970
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  • 10. A case of X-linked alpha-thalassemia/mental retardation syndrome: analysis of hemoglobin by an automated glycated hemoglobin analyzer.
    Kuno T, Ideguchi H, Yoshida N, Masuyama T, Ohta M, Nishimura S, Tasaki H, Miyazaki S, Hara H, Matsumoto K.
    Acta Paediatr Jpn; 1997 Oct; 39(5):615-8. PubMed ID: 9363663
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  • 13. The haemoglobin H disease mental retardation syndrome: molecular studies on the South African case.
    Bowcock AM, van Tonder S, Jenkins T.
    Br J Haematol; 1984 Jan; 56(1):69-78. PubMed ID: 6704328
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  • 14. Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex.
    Wilkie AO, Zeitlin HC, Lindenbaum RH, Buckle VJ, Fischel-Ghodsian N, Chui DH, Gardner-Medwin D, MacGillivray MH, Weatherall DJ, Higgs DR.
    Am J Hum Genet; 1990 Jun; 46(6):1127-40. PubMed ID: 2339705
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  • 17. Molecular genetic study of japanese patients with X-linked alpha-thalassemia/mental retardation syndrome (ATR-X).
    Wada T, Kubota T, Fukushima Y, Saitoh S.
    Am J Med Genet; 2000 Sep 18; 94(3):242-8. PubMed ID: 10995512
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  • 19. Thalassemia types in Southern Sardinia.
    Cao A, Galanello R, Furbetta M.
    Birth Defects Orig Artic Ser; 1982 Sep 18; 18(7):157-64. PubMed ID: 6186310
    [No Abstract] [Full Text] [Related]

  • 20. First occurrence of Hb H in Hungary.
    Horányi M, Földi J, Szelényi JG, Hollán SR, István L, Orkin SH.
    Haematologia (Budap); 1986 Sep 18; 19(3):193-5. PubMed ID: 3781353
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