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 *

116 related articles for article (PubMed ID: 14663844)

  • 1. Analysis of CFTR mutation screening in cases of isolated fetal echogenic bowel in the South Australian population.
    Nicholls CM; Nelson PV; Poplawski NK; Chin SJ; Fong BA; Solly PB; Fietz MJ; Fletcher JM
    Prenat Diagn; 2003 Dec; 23(12):1023-5. PubMed ID: 14663844
    [No Abstract]   [Full Text] [Related]  

  • 2. Incidence and Carrier Frequency of CFTR Gene Mutations in Pregnancies With Echogenic Bowel in Nova Scotia and Prince Edward Island.
    Miller ME; Allen VM; Brock JK
    J Obstet Gynaecol Can; 2018 Jul; 40(7):896-902. PubMed ID: 29503250
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Bayesian risk assessment for autosomal recessive diseases: fetal echogenic bowel with one or no detectable CFTR mutation.
    Ogino S; Wilson RB; Grody WW
    J Med Genet; 2004 May; 41(5):e70. PubMed ID: 15121798
    [No Abstract]   [Full Text] [Related]  

  • 4. Focus on cystic fibrosis and other disorders evidenced in fetuses with sonographic finding of echogenic bowel: 16-year report from Brittany, France.
    Scotet V; Duguépéroux I; Audrézet MP; Audebert-Bellanger S; Muller M; Blayau M; Férec C
    Am J Obstet Gynecol; 2010 Dec; 203(6):592.e1-6. PubMed ID: 20932506
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Towards an improved antenatal screening for cystic fibrosis].
    Serre JL; Feingold J; Simon-Bouy B; Muller F
    Rev Epidemiol Sante Publique; 2003 Apr; 51(2):245-53. PubMed ID: 12876510
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Calculating posterior cystic fibrosis risk with echogenic bowel and one characterized cystic fibrosis mutation: avoiding pitfalls in the risk calculations.
    Hodge SE; Lebo RV; Yesley AR; Cheney SM; Angle H; Milunsky J
    Am J Med Genet; 1999 Feb; 82(4):329-35. PubMed ID: 10051167
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cystic fibrosis mutations with widely variable phenotype: the D1152H example.
    Mussaffi H; Prais D; Mei-Zahav M; Blau H
    Pediatr Pulmonol; 2006 Mar; 41(3):250-4. PubMed ID: 16429425
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hyperechogenic fetal bowel as a marker of fetal cystic fibrosis].
    Sukupová M; Dhaifalah I; Adamík Z; Havalová J
    Ceska Gynekol; 2015 Jan; 80(1):20-4. PubMed ID: 25723074
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mid-trimester hyperechogenic bowel in a fetus of Turkish origin carrying a rarely seen mutation of cystic fibrosis.
    Kazandi M; Turan V; Selvi Demirtas G; Akercan F; Aykut A; Ozkinay F
    Arch Iran Med; 2012 Jul; 15(7):449-51. PubMed ID: 22724884
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Predicting the risk of cystic fibrosis with echogenic fetal bowel and one cystic fibrosis mutation.
    Bosco AF; Norton ME; Lieberman E
    Obstet Gynecol; 1999 Dec; 94(6):1020-3. PubMed ID: 10576193
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal Ultrasound Suspicion of Cystic Fibrosis in a Multiethnic Population: Is Extensive
    Mekki C; Aissat A; Mirlesse V; Mayer Lacrosniere S; Eche E; Le Floch A; Whalen S; Prud'Homme C; Remus C; Funalot B; Castaigne V; Fanen P; de Becdelièvre A
    Genes (Basel); 2021 Apr; 12(5):. PubMed ID: 33946859
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Comprehensive description of CFTR genotypes and ultrasound patterns in 694 cases of fetal bowel anomalies: a revised strategy.
    de Becdelièvre A; Costa C; Jouannic JM; LeFloch A; Giurgea I; Martin J; Médina R; Boissier B; Gameiro C; Muller F; Goossens M; Alberti C; Girodon E
    Hum Genet; 2011 Apr; 129(4):387-96. PubMed ID: 21184098
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hyperechogenic fetal bowel: counseling difficulties.
    Marcus-Soekarman D; Offermans J; Van den Ouweland AM; Mulder AL; Muntjewerff N; Vossen M; Kleijer W; Schrander-Stumpel C; Dooijes D
    Eur J Med Genet; 2005; 48(4):421-5. PubMed ID: 16378926
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R; Kianishirazi R; Cassiman JJ; Zamani M; Cuppens H
    J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CFTR DeltaF508 mutation detection from dried blood samples in the first trimester of pregnancy: a possible routine prenatal screening strategy for cystic fibrosis?
    Konialis CP; Hagnefelt B; Kazamia C; Karapanou S; Pangalos C
    Fetal Diagn Ther; 2007; 22(1):41-4. PubMed ID: 17003555
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Notable contribution of large CFTR gene rearrangements to the diagnosis of cystic fibrosis in fetuses with bowel anomalies.
    de Becdelièvre A; Costa C; LeFloch A; Legendre M; Jouannic JM; Vigneron J; Bresson JL; Gobin S; Martin J; Goossens M; Girodon E
    Eur J Hum Genet; 2010 Oct; 18(10):1166-9. PubMed ID: 20512161
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Geographic distribution of cystic fibrosis transmembrane regulator gene mutations in Saudi Arabia.
    Banjar H
    East Mediterr Health J; 1999 Nov; 5(6):1230-5. PubMed ID: 11924117
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Nonvisualization of fetal gallbladder increases the risk of cystic fibrosis.
    Duguépéroux I; Scotet V; Audrézet MP; Saliou AH; Collet M; Blayau M; Schmitt S; Kitzis A; Fresquet F; Müller F; Férec C
    Prenat Diagn; 2012 Jan; 32(1):21-8. PubMed ID: 22052729
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mid-trimester hyperechogenic bowel in a fetus of Japanese origin carrying a new mutation of CFTR gene (L548Q).
    Yamamoto M; Molina-Gomes D; Girodon-Boulandet E; Moulis M; Leroy B; Simon-Bouy B; Selva J; Ville Y
    Prenat Diagn; 2006 Jan; 26(1):6-8. PubMed ID: 16378323
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Predicting the risk of cystic fibrosis with abnormal ultrasound signs of fetal bowel: results of a French molecular collaborative study based on 641 prospective cases.
    Muller F; Simon-Bouy B; Girodon E; Monnier N; Malinge MC; Serre JL;
    Am J Med Genet; 2002 Jun; 110(2):109-15. PubMed ID: 12116247
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.