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: 8710781)

  • 1. Prenatal diagnosis of adrenoleukodystrophy by means of mutation analysis.
    Imamura A; Suzuki Y; Song XQ; Fukao T; Shimozawa N; Orii T; Kondo N
    Prenat Diagn; 1996 Mar; 16(3):259-61. PubMed ID: 8710781
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DNA-based diagnostics for adrenoleukodystrophy in a large New Zealand family.
    Rowland SA; Dodd A; Roche AL; Manilal S; Kennedy MA; Becroft DM; Tonkin S; Chapman C; Love DR
    N Z Med J; 1996 Aug; 109(1028):312-5. PubMed ID: 8816721
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A point mutation at ATP-binding region of the ALD gene in a family with X-linked adrenoleukodystrophy.
    Matsumoto T; Kondoh T; Masuzaki H; Harada N; Matsusaka T; Kinoshita E; Takeo G; Tsujihata M; Suzuki Y; Tsuji Y
    Jpn J Hum Genet; 1994 Sep; 39(3):345-51. PubMed ID: 7841445
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis of X-linked adrenoleukodystrophy combining biochemical, immunocytochemical and DNA analyses.
    Maier EM; Roscher AA; Kammerer S; Mehnert K; Conzelmann E; Holzinger A
    Prenat Diagn; 1999 Apr; 19(4):364-8. PubMed ID: 10327143
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis in a Chinese family with type Ia glycogen storage disease by PCR-based genetic analysis.
    Lee WJ; Yang CH; Ho ES; Shih A; Lin LY; Lin WH
    Prenat Diagn; 1996 Nov; 16(11):1027-31. PubMed ID: 8953636
    [TBL] [Abstract][Full Text] [Related]  

  • 6. X-linked adrenoleukodystrophy (ALD): a novel mutation of the ALD gene in 6 members of a family presenting with 5 different phenotypes.
    Berger J; Molzer B; Faé I; Bernheimer H
    Biochem Biophys Res Commun; 1994 Dec; 205(3):1638-43. PubMed ID: 7811247
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Prenatal molecular diagnosis of four fetuses at high risk for X-linked adrenoleukodystrophy].
    Ke LF; Wang ZH; Huang HJ; Tu XD; Zeng J; Li B; Yang BS; Lan FH
    Zhonghua Fu Chan Ke Za Zhi; 2008 Jan; 43(1):25-8. PubMed ID: 18366928
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal molecular diagnosis of adrenoleukodystrophy.
    Huang LH; Huang HJ; Yang BS; Tu XD; Zeng J; Li HZ; Xin N; Lan FH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):612-5. PubMed ID: 16331554
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Preimplantation genetic diagnosis of X-linked adrenoleukodystrophy with gender determination using multiple displacement amplification.
    Lledó B; Bernabeu R; Ten J; Galán FM; Cioffi L
    Fertil Steril; 2007 Nov; 88(5):1327-33. PubMed ID: 17498713
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Attitudes toward presymptomatic testing and prenatal diagnosis for adrenoleukodystrophy among affected families.
    Costakos D; Abramson RK; Edwards JG; Rizzo WB; Best RG
    Am J Med Genet; 1991 Dec; 41(3):295-300. PubMed ID: 1789282
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of beta-thalassemia in Egypt: implementing accurate high-tech methods did not reflect much on the outcome.
    Elgawhary S; Elbaradie Sahar MY; Rashad WM; Mosaad M; Abdalla MA; Ezzat G; Wali YA; Elbeshlawy A
    Pediatr Hematol Oncol; 2008 Sep; 25(6):541-8. PubMed ID: 18728973
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular prenatal diagnosis of glycogen storage disease type Ia.
    Qu Y; Abdenur JE; Eng CM; Desnick RJ
    Prenat Diagn; 1996 Apr; 16(4):333-6. PubMed ID: 8734807
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal exclusion of Leigh syndrome due to T8993C mutation in the mitochondrial DNA.
    Leshinsky-Silver E; Perach M; Basilevsky E; Hershkovitz E; Yanoov-Sharav M; Lerman-Sagie T; Lev D
    Prenat Diagn; 2003 Jan; 23(1):31-3. PubMed ID: 12533809
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A rapid and sensitive protocol for prenatal molecular diagnosis of X-linked adrenoleukodystrophy.
    Lan F; Wang Z; Ke L; Xie H; Huang L; Huang H; Tu X; Zheng D; Zeng J; Li H; Xin N; Yang B
    Clin Chim Acta; 2010 Dec; 411(23-24):1992-7. PubMed ID: 20800589
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation analysis of the ALD gene in seven Japanese families with X-linked adrenoleukodystrophy.
    Matsumoto T; Tsuru A; Amamoto N; Shimizu T; Kondoh T; Saitoh N; Tsujii T; Tamagawa K
    J Hum Genet; 2003; 48(3):125-9. PubMed ID: 12624723
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic counselling and prenatal diagnosis of osteogenesis imperfecta caused by paternal mosaicism.
    Lund AM; Schwartz M; Skovby F
    Prenat Diagn; 1996 Nov; 16(11):1032-8. PubMed ID: 8953637
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Reliable co-segregation analysis for prenatal diagnosis and heterozygote detection in Gaucher disease.
    Cormand B; Montfort M; Chabás A; Grinberg D; Vilageliu LL
    Prenat Diagn; 1998 Mar; 18(3):207-12. PubMed ID: 9556036
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Adrenomyeloneuropathy and adrenoleukodystrophy: genetic identity and detection. Apropos of a family].
    Labauge P; Ducros A; Khalaf K; Pages M; Blard JM
    Ann Med Interne (Paris); 1994; 145(1):53-5. PubMed ID: 8192283
    [No Abstract]   [Full Text] [Related]  

  • 19. First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe.
    Boué J; Oberle I; Heilig R; Mandel JL; Moser A; Moser H; Larsen JW; Dumez Y; Boué A
    Hum Genet; 1985; 69(3):272-4. PubMed ID: 3856557
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of congenital myotonic dystrophy and counseling of the pregnant mother: case report and literature review.
    Geifman-Holtzman O; Fay K
    Am J Med Genet; 1998 Jul; 78(3):250-3. PubMed ID: 9677060
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.