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 *

94 related articles for article (PubMed ID: 6984491)

  • 21. Finding genes on the X chromosome by which homo may have become sapiens.
    Turner G
    Am J Hum Genet; 1996 Jun; 58(6):1109-10. PubMed ID: 8651286
    [No Abstract]   [Full Text] [Related]  

  • 22. Gonosomal aberrations and congenital dyschromatopsias.
    François J
    Mod Probl Ophthalmol; 1974; 13(0):231-47. PubMed ID: 4548140
    [No Abstract]   [Full Text] [Related]  

  • 23. Linkage data on affective disorders in an epidemiologic context.
    Gershon ES; Goldin LR
    Genet Epidemiol; 1989; 6(1):201-9. PubMed ID: 2567258
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The effects of variable age-of-onset and diagnostic criteria on the estimates of linkage: an example using manic-depressive illness and color blindness.
    Morton LA; Kidd KK
    Soc Biol; 1980; 27(1):1-10. PubMed ID: 6974894
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Linkage analyses in families with nephrogenic diabetes insipidus.
    Knoers NV; van der Heyden H; van Oost BA; Monnens L; Willems J; Ropers HH
    Prog Clin Biol Res; 1989; 305():149-55. PubMed ID: 2569742
    [No Abstract]   [Full Text] [Related]  

  • 26. [Norrie syndrome: identification of carriers by segregation analysis with flanking DNA markers].
    Körner J; Uhlhaas S; Neugebauer M; Gal A
    Fortschr Ophthalmol; 1989; 86(1):78-81. PubMed ID: 2566566
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Chromosomal rearrangement segregating with adrenoleukodystrophy: a molecular analysis.
    Sack GH; Alpern M; Webster T; Feil RP; Morrell JC; Chen G; Chen W; Caskey CT; Moser HW
    Proc Natl Acad Sci U S A; 1993 Oct; 90(20):9489-93. PubMed ID: 8415728
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [X-chromosome recessive lymphoproliferative disease (XLP): molecular genetic studies].
    Schuster V; Grimm T; Kress W; Seidenspinner S; Belohradsky BH; Müller P; Kreth HW
    Klin Padiatr; 1995; 207(5):271-6. PubMed ID: 7500602
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Fragile X syndrome: a unique mutation in man.
    Nussbaum RL; Ledbetter DH
    Annu Rev Genet; 1986; 20():109-45. PubMed ID: 3545058
    [No Abstract]   [Full Text] [Related]  

  • 30. Amish study, IV: Genetic linkage study of pedigrees of bipolar probands.
    Kidd KK; Egeland JA; Molthan L; Pauls DL; Kruger SD; Messner KH
    Am J Psychiatry; 1984 Sep; 141(9):1042-8. PubMed ID: 6331772
    [TBL] [Abstract][Full Text] [Related]  

  • 31. X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of Xq.
    Schwartz M; Haim M; Skarsholm D
    Clin Genet; 1990 Oct; 38(4):281-6. PubMed ID: 1980096
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mental retardation, megalotestes and a marker X chromosome.
    Fitzsimmons J; McLachlan JI; Fitzsimmons E; Cooke P
    Practitioner; 1982 Apr; 226(1366):735-41. PubMed ID: 6953399
    [No Abstract]   [Full Text] [Related]  

  • 33. Severe X-linked Charcot-Marie-Tooth neuropathy due to new mutations [G59R(G-->C), W44X(G-->A)] in the connexin 32 gene.
    Felice KJ; Seltzer WK
    Eur Neurol; 2000; 44(1):61-3. PubMed ID: 10894999
    [No Abstract]   [Full Text] [Related]  

  • 34. Brief report: linkage between G6PD and fragile-X syndrome.
    Filippi G; Rinaldi A; Archidiacono N; Rocchi M; Balazs I; Siniscalco M
    Am J Med Genet; 1983 May; 15(1):113-9. PubMed ID: 6602550
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Reply to Inglehearn.
    Bergen AA; Pinckers AJ
    Am J Hum Genet; 1998 Oct; 63(4):1232-4. PubMed ID: 9758609
    [No Abstract]   [Full Text] [Related]  

  • 36. Genes and colour blindness.
    Lancet; 1990 Feb; 335(8684):263-4. PubMed ID: 1967724
    [No Abstract]   [Full Text] [Related]  

  • 37. [Etiology of numerical and structural aberrations of the X chromosome. A study with highly polymorphic DNA markers].
    Lorda-Sanchez I; Schinzel AA
    Ergeb Inn Med Kinderheilkd; 1993; 61():57-121. PubMed ID: 7900996
    [No Abstract]   [Full Text] [Related]  

  • 38. Schizoaffective disorders. Results of a genetic investigation, I.
    Angst J; Felder W; Lohmeyer B
    J Affect Disord; 1979 Jun; 1(2):139-53. PubMed ID: 162495
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Re: Psychoses occurring in relation to sex chromosomal anomalies.
    Crow TJ
    J Ment Defic Res; 1990 Apr; 34 ( Pt 2)():211. PubMed ID: 2342096
    [No Abstract]   [Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 5.