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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

67 related articles for article (PubMed ID: 3931215)

  • 21. XXY male with X-linked dominant chondrodysplasia punctata (Happle syndrome).
    Sutphen R; Amar MJ; Kousseff BG; Toomey KE
    Am J Med Genet; 1995 Jul; 57(3):489-92. PubMed ID: 7677157
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetic variants of thyroxine-binding globulin (TBG).
    Rivas ML; Merritt AD; Oliner L
    Birth Defects Orig Artic Ser; 1971 May; 7(6):34-41. PubMed ID: 5006142
    [TBL] [Abstract][Full Text] [Related]  

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

  • 24. [Familial thyroxine-binding globulin deficiency].
    Iino S
    Ryoikibetsu Shokogun Shirizu; 1993; (1):194-5. PubMed ID: 7757555
    [No Abstract]   [Full Text] [Related]  

  • 25. Linkage analysis in three families with nonspecific X-linked mental retardation.
    Claes S; Gu XX; Legius E; Lorenzetti E; Marynen P; Fryns JP; Cassiman JJ; Raeymaekers P
    Am J Med Genet; 1996 Jul; 64(1):137-46. PubMed ID: 8826464
    [TBL] [Abstract][Full Text] [Related]  

  • 26. X-linked dominant chondrodysplasia punctata: a case report and family studies.
    Mueller RF; Crowle PM; Jones RA; Davison BC
    Am J Med Genet; 1985 Jan; 20(1):137-44. PubMed ID: 4038582
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Heritable skewed X-chromosome inactivation leads to haemophilia A expression in heterozygous females.
    Renault NK; Dyack S; Dobson MJ; Costa T; Lam WL; Greer WL
    Eur J Hum Genet; 2007 Jun; 15(6):628-37. PubMed ID: 17342157
    [TBL] [Abstract][Full Text] [Related]  

  • 28. X-linked laterality sequence in a family with carrier manifestations.
    Mikkilä SP; Janas M; Karikoski R; Tarkkila T; Simola KO
    Am J Med Genet; 1994 Feb; 49(4):435-8. PubMed ID: 8160739
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A locus for axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26.
    Priest JM; Fischbeck KH; Nouri N; Keats BJ
    Genomics; 1995 Sep; 29(2):409-12. PubMed ID: 8666389
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [A family with thyroxine-binding globulin deficiency].
    Mitsuno M; Takada H; Imashuku S; Kusunoki T; Miyazaki T
    Horumon To Rinsho; 1975 Jun; 23(6):517-20. PubMed ID: 807444
    [No Abstract]   [Full Text] [Related]  

  • 31. Linkage of thyroxine-binding globulin deficiency to other X-chromosome loci.
    Bode HH; Rothman KJ; Danon M
    J Clin Endocrinol Metab; 1973 Jul; 37(1):25-9. PubMed ID: 4197606
    [No Abstract]   [Full Text] [Related]  

  • 32. Inherited thyroxine-binding globulin abnormalities in man.
    Refetoff S
    Endocr Rev; 1989 Aug; 10(3):275-93. PubMed ID: 2506004
    [No Abstract]   [Full Text] [Related]  

  • 33. [Hereditary thyroxine-binding globulin deficiency combined with hypertrophic obstructive cardiomyopathy].
    Bohner J; Eichstädt H; Wahl R; Kallee E
    Verh Dtsch Ges Inn Med; 1978; (84):666-70. PubMed ID: 105495
    [No Abstract]   [Full Text] [Related]  

  • 34. Protein deficiency in three generations of one family.
    Zauber NP; Kudryk AB
    N J Med; 1988 Oct; 85(10):805-7. PubMed ID: 3226628
    [No Abstract]   [Full Text] [Related]  

  • 35. Increased serum thyroxine-binding globulin capacity: inheritance and linkage relationships.
    Fialkow PJ; Giblett ER; Musa B
    J Clin Endocrinol Metab; 1970 Jan; 30(1):66-70. PubMed ID: 4982599
    [No Abstract]   [Full Text] [Related]  

  • 36. X-chromosome linked inheritance of thyroxine-binding globulin deficiency.
    Nikolai TF; Seal US
    J Clin Endocrinol Metab; 1967 Nov; 27(11):1515-20. PubMed ID: 4965464
    [No Abstract]   [Full Text] [Related]  

  • 37. X-chromosome linked inheritance of elevated thyroxine-binding globulin in association with goiter.
    Shane SR; Seal US; Jones JE
    J Clin Endocrinol Metab; 1971 May; 32(5):587-94. PubMed ID: 4996058
    [No Abstract]   [Full Text] [Related]  

  • 38. [Thyroxine binding globulin deficiency excluding thyroid pathology].
    Massol J; Humbert P; Lestradet C; Narboni G
    Presse Med; 1984 May; 13(20):1277. PubMed ID: 6232592
    [No Abstract]   [Full Text] [Related]  

  • 39. Familial thyroxine-binding globulin deficiency with neurological abnormalities.
    Shita A; Leroy C; Tagnon A; Chanoine F; Henoumont Y; Gillerot Y
    Acta Clin Belg; 1981; 36(6):313-4. PubMed ID: 6173980
    [No Abstract]   [Full Text] [Related]  

  • 40. [Cretinism associated with thyroxine binding globulin deficiency in an infant].
    Niimi H; Sasaki N; Matsutani T
    Horumon To Rinsho; 1975 Jun; 23(6):521-4. PubMed ID: 807445
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.