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 *

152 related articles for article (PubMed ID: 436221)

  • 1. Familial occurrence of mitral valve prolapse in X-linked muscular dystrophy.
    Biddison JH; Dembo DH; Spalt H; Hayes MG; LeDoux CW
    Circulation; 1979 Jun; 59(6):1299-304. PubMed ID: 436221
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitral valve prolapse syndrome in children with Duchenne's progressive muscular dystrophy.
    Sanyal SK; Leung RK; Tierney RC; Gilmartin R; Pitner S
    Pediatrics; 1979 Jan; 63(1):116-23. PubMed ID: 440788
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Atrioventricular block and supraventricular arrhythmias with X-linked muscular dystrophy.
    ul Hassan Z; Fastabend CP; Mohanty PK; Isaacs ER
    Circulation; 1979 Dec; 60(6):1365-9. PubMed ID: 498463
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The genetics of mitral valve prolapse.
    Grau JB; Pirelli L; Yu PJ; Galloway AC; Ostrer H
    Clin Genet; 2007 Oct; 72(4):288-95. PubMed ID: 17850623
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitral valve prolapse related to geometrical changes of the heart in cases of progressive muscular dystrophy.
    Yazawa Y
    Clin Cardiol; 1984 Apr; 7(4):198-204. PubMed ID: 6525776
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Intrafamilial variability of X-linked progressive muscular dystrophy. Mild and acute form of X-linked muscular dystrophy in the same family.
    Hausmanowa-Petrusewicz I; Borkowska J
    J Neurol; 1978 Apr; 218(1):43-50. PubMed ID: 77317
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Screening of TGFBR1, TGFBR2, and FLNA in familial mitral valve prolapse.
    Aalberts JJ; van Tintelen JP; Oomen T; Bergman JE; Halley DJ; Jongbloed JD; Suurmeijer AJ; van den Berg MP
    Am J Med Genet A; 2014 Jan; 164A(1):113-9. PubMed ID: 24243761
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The causative mechanisms of mitral valve prolapse in progressive muscular dystrophy in reference to thorax and thoracic spine deformities and left ventricular dysfunction.
    Yazawa Y; Ohtaki E; Nagai T; Hayashi S; Hosokawa O; Watanabe K; Shibata A; Takasawa N
    Jpn Circ J; 1984 Apr; 48(4):321-7. PubMed ID: 6716630
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.
    Kingston HM; Thomas NS; Pearson PL; Sarfarazi M; Harper PS
    J Med Genet; 1983 Aug; 20(4):255-8. PubMed ID: 6620324
    [TBL] [Abstract][Full Text] [Related]  

  • 10. New locus for autosomal dominant mitral valve prolapse on chromosome 13: clinical insights from genetic studies.
    Nesta F; Leyne M; Yosefy C; Simpson C; Dai D; Marshall JE; Hung J; Slaugenhaupt SA; Levine RA
    Circulation; 2005 Sep; 112(13):2022-30. PubMed ID: 16172273
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in DCHS1 cause mitral valve prolapse.
    Durst R; Sauls K; Peal DS; deVlaming A; Toomer K; Leyne M; Salani M; Talkowski ME; Brand H; Perrocheau M; Simpson C; Jett C; Stone MR; Charles F; Chiang C; Lynch SN; Bouatia-Naji N; Delling FN; Freed LA; Tribouilloy C; Le Tourneau T; LeMarec H; Fernandez-Friera L; Solis J; Trujillano D; Ossowski S; Estivill X; Dina C; Bruneval P; Chester A; Schott JJ; Irvine KD; Mao Y; Wessels A; Motiwala T; Puceat M; Tsukasaki Y; Menick DR; Kasiganesan H; Nie X; Broome AM; Williams K; Johnson A; Markwald RR; Jeunemaitre X; Hagege A; Levine RA; Milan DJ; Norris RA; Slaugenhaupt SA
    Nature; 2015 Sep; 525(7567):109-13. PubMed ID: 26258302
    [TBL] [Abstract][Full Text] [Related]  

  • 12. X-linked muscular dystrophy.
    Furukawa T; Peter JB
    Ann Neurol; 1977 Nov; 2(5):414-6. PubMed ID: 569459
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm.
    Lindenbaum RH; Clarke G; Patel C; Moncrieff M; Hughes JT
    J Med Genet; 1979 Oct; 16(5):389-92. PubMed ID: 513085
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetics of syndromic and non-syndromic mitral valve prolapse.
    Le Tourneau T; Mérot J; Rimbert A; Le Scouarnec S; Probst V; Le Marec H; Levine RA; Schott JJ
    Heart; 2018 Jun; 104(12):978-984. PubMed ID: 29352010
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Echinocytes in families with Duchenne muscular dystrophy.
    Soltan HC
    J Med Genet; 1977 Aug; 14(4):276-8. PubMed ID: 926140
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy.
    Murray JM; Davies KE; Harper PS; Meredith L; Mueller CR; Williamson R
    Nature; 1982 Nov; 300(5887):69-71. PubMed ID: 6982420
    [No Abstract]   [Full Text] [Related]  

  • 17. Molecular deletion analysis in Duchenne muscular dystrophy.
    Thomas NS; Ray PN; Worton RG; Harper PS
    J Med Genet; 1986 Dec; 23(6):509-15. PubMed ID: 2879923
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome.
    Brown CS; Pearson PL; Thomas NS; Sarfarazi M; Harper PS; Shaw DJ
    J Med Genet; 1985 Jun; 22(3):179-81. PubMed ID: 2989525
    [TBL] [Abstract][Full Text] [Related]  

  • 19. X-linked Duchenne muscular dystrophy in an unusual family with manifesting carriers.
    Kaladhar Reddy B; Anandavalli TE; Reddi OS
    Hum Genet; 1984; 67(4):460-2. PubMed ID: 6490012
    [TBL] [Abstract][Full Text] [Related]  

  • 20. X-linked gene loci and muscular dystrophy.
    Grounds MD
    Aust J Exp Biol Med Sci; 1981 Oct; 59(Pt 5):617-22. PubMed ID: 6459775
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.