BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

77 related articles for article (PubMed ID: 7163218)

  • 21. Discriminant analysis of ribosomal protein synthesis findings in carrier detection of Duchenne muscular dystrophy.
    Ionasescu V; Burmeister L; Hanson J
    Am J Med Genet; 1980; 5(1):5-12. PubMed ID: 7395900
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Carrier detection of hemophilia A in a Mexican population by two Bcl I polymorphisms.
    Carrillo Pérez MD; Fragoso Herrera R; Cisneros Vega B; Amparo Esparza M; Cantú JM; Montañez Ojeda C
    Arch Med Res; 1993; 24(2):139-42. PubMed ID: 7903882
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Use of Intron 1 and 22 inversions and linkage analysis in carrier detection of hemophilia A in Indians.
    Ahmed R; Kannan M; Biswas A; Ranjan R; Choudhry VP; Saxena R
    Clin Chim Acta; 2006 Mar; 365(1-2):109-12. PubMed ID: 16129422
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Tests of serum creatine phosphokinase activity in patients with progressive muscular dystrophy and their relatives for the detection of genetic carriers].
    László A; Salgó L
    Orv Hetil; 1981 Jun; 122(24):1453-6. PubMed ID: 7290660
    [No Abstract]   [Full Text] [Related]  

  • 25. Carrier detection in Duchenne and Becker muscular dystrophy using dinucleotide repeat polymorphisms. A study in Mexican families.
    Arenas D; Coral R; Cisneros B; Peñaloza L; Salamanca F; Kofman S; Mercado R; Méndez J; Martínez C; Montañez C
    Arch Med Res; 1996; 27(2):151-6. PubMed ID: 8696057
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Perspectives and molecular diagnosis of Duchenne and Becker muscular dystrophies.
    Prior TW
    Clin Lab Med; 1995 Dec; 15(4):927-41. PubMed ID: 8838231
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Carrier detection and prenatal diagnosis of hemophilia A in a Korean population by PCR-based analysis of the BclI/intron 18 and St14 VNTR polymorphisms.
    Choi YM; Hwang D; Choe J; Jun JK; Kim EJ; Moon SY; Cho S
    J Hum Genet; 2000; 45(4):218-23. PubMed ID: 10944851
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [DNA and dystrophin analysis in Duchenne's and Becker's disease; benefit to the patient].
    Jennekens FG; Ippel PF
    Ned Tijdschr Geneeskd; 1993 Jan; 137(2):61-3. PubMed ID: 8421528
    [No Abstract]   [Full Text] [Related]  

  • 29. Carrier detection and prenatal diagnosis of hemophilia in developing countries.
    Peyvandi F
    Semin Thromb Hemost; 2005 Nov; 31(5):544-54. PubMed ID: 16276463
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A probable sex difference in some mutation rates.
    Vogel F
    Am J Hum Genet; 1977 May; 29(3):312-9. PubMed ID: 868880
    [No Abstract]   [Full Text] [Related]  

  • 31. [Population and molecular-genetic aspects of hemophilia A and B in Uzbekistan].
    Boboev KT
    Tsitol Genet; 2008; 42(2):51-4. PubMed ID: 18630121
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Triple parameter discriminant analysis and carriers of haemophilia.
    Marshall LR; Stenhouse NS
    Thromb Haemost; 1979 Aug; 42(2):810-2. PubMed ID: 505384
    [No Abstract]   [Full Text] [Related]  

  • 33. Carrier testing of children for two X linked diseases in a family based setting: a retrospective long term psychosocial evaluation.
    Järvinen O; Aalto AM; Lehesjoki AE; Lindlöf M; Söderling I; Uutela A; Kääriäinen H
    J Med Genet; 1999 Aug; 36(8):615-20. PubMed ID: 10465112
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Improved assay for genotyping haemophilia A carriers with intron 22 dinucleotide repeat marker.
    Saha A; Mukherjee S; Ray K
    Haemophilia; 2006 Mar; 12(2):200-1. PubMed ID: 16476099
    [No Abstract]   [Full Text] [Related]  

  • 35. Utility of a (GT) dinucleotide repeat in intron 1 of the factor 8 gene for haemophilia A carrier diagnosis.
    Tizzano E; Venceslá A; Cornet M; Baena M; Baiget M
    Haemophilia; 2005 Mar; 11(2):142-4. PubMed ID: 15810916
    [TBL] [Abstract][Full Text] [Related]  

  • 36. DNA polymorphisms for carrier detection of hemophilia in Thailand.
    Chuansumrit A; Goodeve A; Sasanakul W; Peake IR; Pintadit P; Hathirat P; Preston FE; Isarangkul P
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():201-6. PubMed ID: 8629107
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Direct molecular genetic diagnosis and heterozygote identification in X-linked Emery-Dreifuss muscular dystrophy by heteroduplex analysis.
    Wulff K; Ebener U; Wehnert CS; Ward PA; Reuner U; Hiebsch W; Herrmann FH; Wehnert M
    Dis Markers; 1997 Apr; 13(2):77-86. PubMed ID: 9160182
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Carrier analysis for hemophilia A: ideal versus acceptable.
    Husain N
    Expert Rev Mol Diagn; 2009 Apr; 9(3):203-7. PubMed ID: 19379077
    [No Abstract]   [Full Text] [Related]  

  • 39. Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy.
    Tuffery S; Moine P; Sarda P; Lefort G; Boulot P; Demaille J; Claustres M
    Genet Couns; 1994; 5(2):183-5. PubMed ID: 7917130
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The molecular basis of hemophilia A and the present status of carrier and antenatal diagnosis of the disease.
    Kazazian HH
    Thromb Haemost; 1993 Jul; 70(1):60-2. PubMed ID: 8236115
    [No Abstract]   [Full Text] [Related]  

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