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 *

130 related articles for article (PubMed ID: 21242988)

  • 1. A possible genetic answer to a recently reported novel phenotype.
    Khan K; Ali M; Inglehearn C
    Eye (Lond); 2011 Apr; 25(4):529; author reply 529-30. PubMed ID: 21242988
    [No Abstract]   [Full Text] [Related]  

  • 2. Elucidation of the gene defect in Marfan syndrome. Success by two complementary research strategies.
    Peltonen L; Kainulainen K
    FEBS Lett; 1992 Jul; 307(1):116-21. PubMed ID: 1639186
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Anthropometric parameters in assessment of patients with Marfan syndrome or with Marfan phenotype].
    Głowacki M; Ignyś A; Szulc A; Kraśny I; Krawczyński M
    Chir Narzadow Ruchu Ortop Pol; 1998; 63(4):373-8. PubMed ID: 9857556
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A linkage study of the Marfan syndrome.
    Schleutermann DA; Murdoch JL; Walker BA; Bias WB; Chase GA; Freidhoff LB; McKusick VA
    Clin Genet; 1976 Jul; 10(1):51-3. PubMed ID: 949864
    [No Abstract]   [Full Text] [Related]  

  • 5. The phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome.
    Burn J; Camm J; Davies MJ; Peltonen L; Schwartz PJ; Watkins H
    Heart; 1997 Aug; 78(2):110-6. PubMed ID: 9326982
    [No Abstract]   [Full Text] [Related]  

  • 6. Analysis of phenotype and genotype information for the diagnosis of Marfan syndrome.
    Sheikhzadeh S; Kade C; Keyser B; Stuhrmann M; Arslan-Kirchner M; Rybczynski M; Bernhardt AM; Habermann CR; Hillebrand M; Mir T; Robinson PN; Berger J; Detter C; Blankenberg S; Schmidtke J; von Kodolitsch Y
    Clin Genet; 2012 Sep; 82(3):240-7. PubMed ID: 21883168
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The genetic basis of aortic disease. Marfan syndrome and beyond.
    Tsipouras P; Silverman DI
    Cardiol Clin; 1999 Nov; 17(4):683-96. PubMed ID: 10589339
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Novel Fibrillin-1 Gene Mutation Leading to Marfan Syndrome in a Korean Girl.
    Nam HK; Nam MH; Ha KS; Rhie YJ; Lee KH
    Ann Clin Lab Sci; 2017 Mar; 47(2):221-225. PubMed ID: 28442527
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The question of heterogeneity in Marfan syndrome.
    Dietz H; Francke U; Furthmayr H; Francomano C; De Paepe A; Devereux R; Ramirez F; Pyeritz R
    Nat Genet; 1995 Mar; 9(3):228-31. PubMed ID: 7773282
    [No Abstract]   [Full Text] [Related]  

  • 10. Genetic testing of the FBN1 gene in Chinese patients with Marfan/Marfan-like syndrome.
    Yang H; Luo M; Chen Q; Fu Y; Zhang J; Qian X; Sun X; Fan Y; Zhou Z; Chang Q
    Clin Chim Acta; 2016 Aug; 459():30-35. PubMed ID: 27234404
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Marfan syndrome locus: confirmation of assignment to chromosome 15 and identification of tightly linked markers at 15q15-q21.3.
    Dietz HC; Pyeritz RE; Hall BD; Cadle RG; Hamosh A; Schwartz J; Meyers DA; Francomano CA
    Genomics; 1991 Feb; 9(2):355-61. PubMed ID: 2004786
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype-phenotype correlations in FBN1 exons 24-40.
    Tiecke F; Katzke S; Booms P; Robinson PN; Neumann L; Godfrey M; Mathews KR; Scheuner M; Hinkel GK; Brenner RE; Hövels-Gürich HH; Hagemeier C; Fuchs J; Skovby F; Rosenberg T
    Eur J Hum Genet; 2001 Jan; 9(1):13-21. PubMed ID: 11175294
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Marfan syndrome: light at the end of the tunnel?
    Tsipouras P
    Am J Hum Genet; 1990 Apr; 46(4):643-5. PubMed ID: 2316516
    [No Abstract]   [Full Text] [Related]  

  • 14. Heterozygous nonsense variant of CHD8 in a patient with forme-fruste Marfan syndrome and intellectual disability.
    Yamada M; Yamaguchi Y; Uehara T; Yagihashi T; Kosaki K
    Congenit Anom (Kyoto); 2021 Jan; 61(1):30-32. PubMed ID: 32951261
    [No Abstract]   [Full Text] [Related]  

  • 15. Marfan syndrome, inherited aortopathies and exercise: what is the right answer?
    Cheng A; Owens D
    Heart; 2015 May; 101(10):752-7. PubMed ID: 25911666
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The molecular basis of Marfan syndrome.
    Maslen CL; Glanville RW
    DNA Cell Biol; 1993 Sep; 12(7):561-72. PubMed ID: 8397814
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic testing in Marfan syndrome.
    Child AH; Aragon-Martin JA; Sage K
    Br J Hosp Med (Lond); 2016 Jan; 77(1):38-41. PubMed ID: 26903455
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Co-occurrence of Marfan syndrome and schizophrenia: what can be learned?
    Van Den Bossche MJ; Van Wallendael KL; Strazisar M; Sabbe B; Del-Favero J
    Eur J Med Genet; 2012 Apr; 55(4):252-5. PubMed ID: 22406088
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The 8th international research symposium on the Marfan syndrome and related conditions.
    Pyeritz RE; Loeys B
    Am J Med Genet A; 2012 Jan; 158A(1):42-9. PubMed ID: 22140025
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Homozygosity for a FBN1 missense mutation causes a severe Marfan syndrome phenotype.
    Hogue J; Lee C; Jelin A; Strecker MN; Cox VA; Slavotinek AM
    Clin Genet; 2013 Oct; 84(4):392-3. PubMed ID: 23278365
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.