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 *

124 related articles for article (PubMed ID: 7513888)

  • 21. Preimplantation single-cell analysis of multiple genetic loci by whole-genome amplification.
    Snabes MC; Chong SS; Subramanian SB; Kristjansson K; DiSepio D; Hughes MR
    Proc Natl Acad Sci U S A; 1994 Jun; 91(13):6181-5. PubMed ID: 7517043
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Applications of the polymerase chain reaction (PCR) in diagnosis.
    Fanning S; Joyce C; Corbett A; O'Mullane J; Cryan B
    Ir J Med Sci; 1995; 164(2):116-21. PubMed ID: 7607835
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular and clinical findings in Austrian cystic fibrosis patients with mutations in exon 11 of the CFTR gene.
    Greil I; Wagner K; Eber E; Zach M; Rosenkranz W
    Wien Klin Wochenschr; 1995; 107(15):464-9. PubMed ID: 7545856
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Clinical experience with preimplantation genetic diagnosis of cystic fibrosis (delta F508).
    Ao A; Ray P; Harper J; Lesko J; Paraschos T; Atkinson G; Soussis I; Taylor D; Handyside A; Hughes M; Winston RM
    Prenat Diagn; 1996 Feb; 16(2):137-42. PubMed ID: 8650124
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification of the five most common cystic fibrosis mutations in single cells using a rapid and specific differential amplification system.
    Scobie G; Woodroffe B; Fishel S; Kalsheker N
    Mol Hum Reprod; 1996 Mar; 2(3):203-7. PubMed ID: 9238680
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Segregation of delta F508 and normal CFTR alleles in human sperm.
    Williams C; Davies D; Williamson R
    Hum Mol Genet; 1993 Apr; 2(4):445-8. PubMed ID: 7684944
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel CFTR mutation, 4035delA, detected by non-radioactive SSCP analysis.
    Reiss J; Lenz U; Rininsland F; Ballhausen P; Drews D; Posselt HG
    Hum Genet; 1992 Nov; 90(3):303-4. PubMed ID: 1283151
    [TBL] [Abstract][Full Text] [Related]  

  • 28. HLA-DQA1 typing in Danes by two polymerase chain reaction (PCR) based methods.
    Cowland JB; Madsen HO; Morling N
    Forensic Sci Int; 1995 May; 73(1):1-13. PubMed ID: 7750878
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Single-strand conformation polymorphism (SSCP) analysis of exon 11 of the CFTR gene reliably detects more than one third of non-delta F508 mutations in German cystic fibrosis patients.
    Plieth J; Rininsland F; Schlösser M; Cooper DN; Reiss J
    Hum Genet; 1992 Jan; 88(3):283-7. PubMed ID: 1370807
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders.
    Harper JC; Wells D; Piyamongkol W; Abou-Sleiman P; Apessos A; Ioulianos A; Davis M; Doshi A; Serhal P; Ranieri M; Rodeck C; Delhanty JD
    Prenat Diagn; 2002 Jun; 22(6):525-33. PubMed ID: 12116320
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multiplex PCR of polymorphic markers flanking the CFTR gene; a general approach for preimplantation genetic diagnosis of cystic fibrosis.
    Dreesen JC; Jacobs LJ; Bras M; Herbergs J; Dumoulin JC; Geraedts JP; Evers JL; Smeets HJ
    Mol Hum Reprod; 2000 May; 6(5):391-6. PubMed ID: 10775641
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Frequency of the delta F508 and exon 11 mutations in Norwegian cystic fibrosis patients.
    Eiklid K; Tranebjaerg L; Eiken HG; Pedersen JC; Michalsen H; Fluge G; Schwartz M; Nilsen BR; Bolle R; Skyberg D
    Clin Genet; 1993 Jul; 44(1):12-4. PubMed ID: 7691448
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Simultaneous detection of the two prevalent mutations in the cystic fibrosis gene in Reunion Island.
    Bienvenu T; Bousquet S; Herbulot C; Cartault F; Kaplan JC; Beldjord C
    Hum Mutat; 1993; 2(4):306-8. PubMed ID: 7691353
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Rapid cycle allele-specific amplification: studies with the cystic fibrosis delta F508 locus.
    Wittwer CT; Marshall BC; Reed GH; Cherry JL
    Clin Chem; 1993 May; 39(5):804-9. PubMed ID: 7683581
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A deletion mutation of the cystic fibrosis transmembrane conductance regulator (CFTR) locus: Delta I507.
    Schwarz M; Summers C; Heptinstall L; Newton C; Markham A; Super M
    Adv Exp Med Biol; 1991; 290():393-8. PubMed ID: 1719770
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families.
    Dörk T; Neumann T; Wulbrand U; Wulf B; Kälin N; Maass G; Krawczak M; Guillermit H; Ferec C; Horn G
    Hum Genet; 1992 Feb; 88(4):417-25. PubMed ID: 1371263
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Preimplantation genetic diagnosis of cystic fibrosis (delta F508).
    Ao A; Handyside A; Winston RM
    Eur J Obstet Gynecol Reprod Biol; 1996 Mar; 65(1):7-10. PubMed ID: 8706961
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The delta F508 mutation in mild adult forms of cystic fibrosis (CF).
    Simon-Bouy B; Mornet E; Taillandier A; Serre JL; Boue J; Boue A
    Clin Genet; 1991 Apr; 39(4):304-5. PubMed ID: 1712680
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Analysis of delta F508 mutation in cystic fibrosis pathology specimens.
    Ozgüç M; Tekin A; Erdem H; Yilmaz E; Ayter S; Coşkun T; Can A; Gögüş S; Caglar M; Kale G
    Pediatr Pathol; 1994; 14(3):491-6. PubMed ID: 7520582
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Single intragenic microsatellite preimplantation genetic diagnosis for cystic fibrosis provides positive allele identification of all CFTR genotypes for informative couples.
    Eftedal I; Schwartz M; Bendtsen H; Andersen AN; Ziebe S
    Mol Hum Reprod; 2001 Mar; 7(3):307-12. PubMed ID: 11228252
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.