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Journal Abstract Search

114 related items for PubMed ID: 6891556

  • 21. [Prenatal diagnosis of X-linked adrenal hypoplasia associated with glycerol kinase deficiency].
    Malpuech G, Dastugue B, Giraud G, Jouanel P, Vanlieferinghen P, Carla H.
    J Genet Hum; 1989 Jun; 37(2):155-62. PubMed ID: 2545811
    [Abstract] [Full Text] [Related]

  • 22. Congenital deafness and hypogonadism: a new X-linked recessive disorder.
    Myhre SA, Ruvalcaba RH, Kelley VC.
    Clin Genet; 1982 Dec; 22(6):299-307. PubMed ID: 6819099
    [No Abstract] [Full Text] [Related]

  • 23. Genetic factors in adrenocortical insufficiency.
    Migeon CJ.
    Birth Defects Orig Artic Ser; 1971 May; 7(6):101-7. PubMed ID: 5173152
    [No Abstract] [Full Text] [Related]

  • 24. A family showing apparent X linked inheritance of both anencephaly and spina bifida.
    Jensson O, Arnason A, Gunnarsdottir H, Petursdottir I, Fossdal R, Hreidarsson S.
    J Med Genet; 1988 Apr; 25(4):227-9. PubMed ID: 3285008
    [Abstract] [Full Text] [Related]

  • 25. [X-linked congenital adrenal hypoplasia].
    Kaji M.
    Nihon Rinsho; 2006 May 28; Suppl 1():556-8. PubMed ID: 16776214
    [No Abstract] [Full Text] [Related]

  • 26. X-linked recessive inheritance of sensorineural hearing loss expressed during adolescence.
    Pelletier LP, Tanguay RB.
    Am J Hum Genet; 1975 Sep 28; 27(5):609-13. PubMed ID: 1163535
    [Abstract] [Full Text] [Related]

  • 27. Congenital adrenal hypoplasia in a male with gonadotropin deficiency.
    Ferrández A, Fuertes J, Martinez MP, Atarés M, Zubillaga P.
    Helv Paediatr Acta; 1984 Oct 28; 39(4):379-84. PubMed ID: 6543850
    [Abstract] [Full Text] [Related]

  • 28. X-linked Leigh's syndrome.
    Benke PJ, Parker JC, Lubs ML, Benkendorf J, Feuer AE.
    Hum Genet; 1982 Oct 28; 62(1):52-9. PubMed ID: 6891369
    [Abstract] [Full Text] [Related]

  • 29. [Clinical features of 9 patients with X-linked adrenal hypoplasia congenita caused by DAX1/NR0B1 gene mutations].
    Fu Y, Nie M, Xia WB, Lu L, Mao JF, Pan H, Wu XY, Zhao WG.
    Zhonghua Yi Xue Za Zhi; 2010 Aug 10; 90(30):2119-22. PubMed ID: 21029627
    [Abstract] [Full Text] [Related]

  • 30. Congenital adrenal hypoplasia: clinical spectrum, experience with hormonal diagnosis, and report on new point mutations of the DAX-1 gene.
    Peter M, Viemann M, Partsch CJ, Sippell WG.
    J Clin Endocrinol Metab; 1998 Aug 10; 83(8):2666-74. PubMed ID: 9709929
    [Abstract] [Full Text] [Related]

  • 31. New mutations of DAX-1 genes in two Japanese patients with X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism.
    Yanase T, Takayanagi R, Oba K, Nishi Y, Ohe K, Nawata H.
    J Clin Endocrinol Metab; 1996 Feb 10; 81(2):530-5. PubMed ID: 8636263
    [Abstract] [Full Text] [Related]

  • 32. Elevated thyroxine-binding globulin with X-chromosome linked inheritance.
    Buchanan BD, Hagen GA.
    Clin Endocrinol (Oxf); 1979 Dec 10; 11(6):665-9. PubMed ID: 119595
    [Abstract] [Full Text] [Related]

  • 33. The calculation of genetic risks in X-linked recessive conditions using programmable calculators.
    Winter RM.
    Clin Genet; 1980 Feb 10; 17(2):171-5. PubMed ID: 7363503
    [Abstract] [Full Text] [Related]

  • 34. [Adrenal hypoplasia congenita: four new cases in children].
    Pélissier P, Merlin E, Prieur F, David M, Malpuech G, Forest MG, Morel Y, Nicolino M, Richard O, Stéphan JL.
    Arch Pediatr; 2005 Apr 10; 12(4):380-4. PubMed ID: 15808425
    [Abstract] [Full Text] [Related]

  • 35. A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
    Tranebjaerg L, Schwartz C, Eriksen H, Andreasson S, Ponjavic V, Dahl A, Stevenson RE, May M, Arena F, Barker D.
    J Med Genet; 1995 Apr 10; 32(4):257-63. PubMed ID: 7643352
    [Abstract] [Full Text] [Related]

  • 36. Ichthyosis vulgaris showing features of the autosomal dominant and X-linked recessive variants in the same family.
    Mevorah B, Frenk E, Pescia G.
    Clin Genet; 1978 Jun 10; 13(6):462-70. PubMed ID: 668182
    [Abstract] [Full Text] [Related]

  • 37. Taurodontism and enamel hypomaturation associated with X-linked abnormalities.
    Gage JP.
    Clin Genet; 1978 Sep 10; 14(3):159-64. PubMed ID: 568045
    [Abstract] [Full Text] [Related]

  • 38. Contrasting effects of subcutaneous pulsatile GnRH therapy in congenital adrenal hypoplasia and Kallmann's syndrome.
    Gordon D, Cohen HN, Beastall GH, Hay ID, Thomson JA.
    Clin Endocrinol (Oxf); 1984 Dec 10; 21(6):597-603. PubMed ID: 6439437
    [Abstract] [Full Text] [Related]

  • 39. Familial cytomegalic adrenocortical hypoplasia: an X-linked syndrome of pubertal failure.
    Hay ID, Smail PJ, Forsyth CC.
    Arch Dis Child; 1981 Sep 10; 56(9):715-21. PubMed ID: 7197507
    [Abstract] [Full Text] [Related]

  • 40. Proposed assignment of loci for X-linked adrenal hypoplasia and glycerol kinase genes.
    Hammond J, Howard NJ, Brookwell R, Purvis-Smith S, Wilcken B, Hoogenraad N.
    Lancet; 1985 Jan 05; 1(8419):54. PubMed ID: 2856983
    [No Abstract] [Full Text] [Related]

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