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 *

139 related articles for article (PubMed ID: 2210750)

  • 1. The mutation delta F508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosis.
    Halley DJ; Veeze HJ; Sandkuyl LA; Wesby-van Swaay E; van Damme NH; Deelen WH; Witte JE; Niermeijer MF
    Hum Genet; 1990 Sep; 85(4):407-8. PubMed ID: 2210750
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Frequency of the delta F508 mutation and XV2c,KM19 haplotypes in cystic fibrosis families from The Netherlands: haplotypes without delta F508 still in disequilibrium.
    Scheffer H; Bruinvels DJ; te Meerman GJ; Verlind E; Penninga D; Dankert J; Ten Kate LP; Buys CH
    Hum Genet; 1990 Sep; 85(4):425-7. PubMed ID: 2210761
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prevalence of delta F508 cystic fibrosis carriers in The Netherlands: logistic regression on sex, age, region of residence and number of offspring.
    de Vries HG; Collée JM; de Walle HE; van Veldhuizen MH; Smit Sibinga CT; Scheffer H; ten Kate LP
    Hum Genet; 1997 Jan; 99(1):74-9. PubMed ID: 9003498
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Difference in frequencies of the cystic fibrosis alleles, delta F508 and W1282X, between carriers and patients.
    Kalman YM; Kerem E; Darvasi A; DeMarchi J; Kerem B
    Eur J Hum Genet; 1994; 2(2):77-82. PubMed ID: 8044659
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An abnormal distribution of delta F508 genotypes in cystic fibrosis patient registries.
    Feingold J; Guilloud-Bataille M; De Crozes D
    Ann Genet; 1998; 41(1):31-3. PubMed ID: 9599649
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Frequency of the phenylalanine deletion (delta F508) in the CF gene of Belgian cystic fibrosis patients.
    Wauters JG; Hendrickx J; Coucke P; Vits L; Stuer K; van Schil L; van der Auwera BJ; Van Elsen A; Dumon J; Willems PJ
    Clin Genet; 1991 Feb; 39(2):89-92. PubMed ID: 1673094
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [A molecular study of the delta-F508 mutation and genetic analysis of a sample of cystic fibrosis patients].
    Orozco L; Lezana JL; Chávez M; Valdez H; Moreno M; Carnevale A
    Bol Med Hosp Infant Mex; 1993 Jul; 50(7):457-62. PubMed ID: 7689846
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequency of the F508 deletion in the CFTR gene in Turkish cystic fibrosis patients.
    Hundrieser J; Bremer S; Peinemann F; Stuhrmann M; Hoffknecht N; Wulf B; Schmidtke J; Reiss J; Maass G; Tümmler B
    Hum Genet; 1990 Sep; 85(4):409-10. PubMed ID: 2210752
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The frequency of the delta F508 mutation on cystic fibrosis chromosomes in Israeli families: correlation to CF haplotypes in Jewish communities and Arabs.
    Lerer I; Cohen S; Chemke M; Sanilevich A; Rivlin J; Golan A; Yahav J; Friedman A; Abeliovich D
    Hum Genet; 1990 Sep; 85(4):416-7. PubMed ID: 1976595
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. The deletion F508 is the major gene mutation in a representative Belgian cystic fibrosis population.
    Bonduelle M; Lissens W; Malfroot A; Dab I; Liebaers I
    Hum Genet; 1990 Sep; 85(4):395-6. PubMed ID: 2210742
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The haplotype distribution of the delta F508 mutation in cystic fibrosis families in Scotland.
    McIntosh I; Curtis A; Lorenzo ML; Keston M; Gilfillan AJ; Morris G; Brock DJ
    Hum Genet; 1990 Sep; 85(4):419-20. PubMed ID: 2210756
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular data on cystic fibrosis in Bulgaria.
    Kalaydjieva L; Antov J; Bronzova J; Vladimirova V; Horst J
    Hum Genet; 1990 Sep; 85(4):412-3. PubMed ID: 1976594
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neonatal screening for the cystic fibrosis main mutation delta F508 in Estonia.
    Klaassen T; Teder M; Viikmaa M; Metspalu A
    J Med Screen; 1998; 5(1):16-9. PubMed ID: 9575453
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Diagnostic value of the deletion of the delta F508 gene in cystic fibrosis].
    Fernández García E; Nunes Martínez V; Ibáñez Olias MA; Benítez Ortíz J
    An Esp Pediatr; 1991 Nov; 35(5):307-8. PubMed ID: 1785742
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cystic fibrosis typing with DNA probes and screening for delta F508 deletion in families from southern France.
    Claustres M; Desgeorges M; Kjellberg P; Bellet H; Demaille J; Ramsay M
    Hum Genet; 1990 Sep; 85(4):398-9. PubMed ID: 1976591
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Frequency of the delta F508 mutation and flanking marker haplotypes at the CF locus from 167 Czech families.
    Macek M; Vavrová V; Böhm I; Stuhrmann M; Reis A; Duspivová R; Macek M; Sperling K; Krawczak M; Schmidtke J
    Hum Genet; 1990 Sep; 85(4):417-8. PubMed ID: 2210755
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Distribution of the delta F508 mutation in 194 Spanish cystic fibrosis families.
    Chillón M; Nunes V; Casals T; Giménez FJ; Fernández E; Benítez J; Estivill X
    Hum Genet; 1990 Sep; 85(4):396-7. PubMed ID: 2210743
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Cystic fibrosis in Asturias: an elevated frequency of the delta F508 mutation].
    Coto E; Bousoño C; Menéndez MJ; Cue R; Toral JF; Benavides A; Hernando I; Plasencia A; López-Larrea C
    Med Clin (Barc); 1994 Nov; 103(18):681-3. PubMed ID: 7808073
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Specific gene deletion in patients with cystic fibrosis: pilot study of a small patient cohort].
    Scheurlen W; Jeschke R; Kreth HW
    Padiatr Grenzgeb; 1991; 30(4):275-81. PubMed ID: 1923546
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.