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 *

100 related articles for article (PubMed ID: 7807930)

  • 1. Detection of genetic defects in Menkes disease by direct mutation analysis and its implications in carrier diagnosis.
    Tümer Z; Tønnesen T; Horn N
    J Inherit Metab Dis; 1994; 17(3):267-70. PubMed ID: 7807930
    [No Abstract]   [Full Text] [Related]  

  • 2. High 64Cu uptake and retention values in two clinically atypical Menkes patients.
    Tønnesen T; Garrett C; Gerdes AM
    J Med Genet; 1991 Sep; 28(9):615-8. PubMed ID: 1956061
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical expression of Menkes syndrome in females.
    Gerdes AM; Tønnesen T; Horn N; Grisar T; Marg W; Müller A; Reinsch R; Barton NW; Guiraud P; Joannard A
    Clin Genet; 1990 Dec; 38(6):452-9. PubMed ID: 2289318
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Menkes' X-linked disease: prenatal diagnosis and carrier detection.
    Horn N
    J Inherit Metab Dis; 1983; 6 Suppl 1():59-62. PubMed ID: 6413776
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Menkes disease: underlying genetic defect and new diagnostic possibilities.
    Tümer Z; Horn N
    J Inherit Metab Dis; 1998 Aug; 21(5):604-12. PubMed ID: 9728340
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis of Menkes disease.
    Kaler SG; Tümer Z
    Prenat Diagn; 1998 Mar; 18(3):287-9. PubMed ID: 9556046
    [No Abstract]   [Full Text] [Related]  

  • 7. Menkes X linked disease: heterozygous phenotype in uncloned fibroblast cultures.
    Horn N
    J Med Genet; 1980 Aug; 17(4):257-61. PubMed ID: 7205900
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Postmortem Menkes diagnosis from carrier testing of female relatives.
    Tønnesen T; Silengo M; Gerdes AM; Hansen JC; Reske-Nielsen E; Franceschini P; Horn N
    Clin Genet; 1987 Dec; 32(6):393-7. PubMed ID: 3436089
    [TBL] [Abstract][Full Text] [Related]  

  • 9. X-linked recessive Menkes disease: carrier detection in the case of a partial gene deletion.
    Poulsen L; Horn N; Møller LB
    Clin Genet; 2002 Dec; 62(6):440-8. PubMed ID: 12485191
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ectodermal manifestations in Menkes disease.
    Moore CM; Howell RR
    Clin Genet; 1985 Dec; 28(6):532-40. PubMed ID: 4075564
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fibroblast silver loading for the diagnosis of Menkes disease.
    Verheijen FW; Beerens CE; Havelaar AC; Kleijer WJ; Mancini GM
    J Med Genet; 1998 Oct; 35(10):849-51. PubMed ID: 9783711
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Menkes X-linked disease: prenatal diagnosis of hemizygous males and heterozygous females.
    Horn N
    Prenat Diagn; 1981 Apr; 1(2):107-20. PubMed ID: 7346814
    [TBL] [Abstract][Full Text] [Related]  

  • 13. First trimester prenatal diagnosis of Menkes disease by DNA analysis.
    Tümer Z; Tønnesen T; Böhmann J; Marg W; Horn N
    J Med Genet; 1994 Aug; 31(8):615-7. PubMed ID: 7815418
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphism.
    Wieacker P; Horn N; Pearson P; Wienker TF; McKay E; Ropers HH
    Hum Genet; 1983; 64(2):139-42. PubMed ID: 6576980
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Menkes X linked disease: two clonal cell populations in heterozygotes.
    Horn N; Mooy P; McGuire VM
    J Med Genet; 1980 Aug; 17(4):262-6. PubMed ID: 7205901
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The metallothionein-I gene maps to mouse chromosome 8: implications for human Menkes' disease.
    Cox DR; Palmiter RD
    Hum Genet; 1983; 64(1):61-4. PubMed ID: 6683708
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Picture of the month. Menkes' syndrome.
    Gellis SS; Feingold M; Robertson WC; Joffe A; Packard TJ
    Am J Dis Child; 1979 Aug; 133(8):853-4. PubMed ID: 572633
    [No Abstract]   [Full Text] [Related]  

  • 18. Accumulated experience with prenatal diagnosis of Menkes disease by neutron activation analysis of chorionic villi specimens.
    Heydorn K; Damsgaard E; Horn N
    Biol Trace Elem Res; 1999; 71-72():551-61. PubMed ID: 10676531
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Menkes kinky hair syndrome: a case report.
    Ghosh S; Chaudhuri S
    Dermatol Online J; 2012 Nov; 18(11):4. PubMed ID: 23217945
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase.
    Vulpe C; Levinson B; Whitney S; Packman S; Gitschier J
    Nat Genet; 1993 Jan; 3(1):7-13. PubMed ID: 8490659
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.