BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 2739665)

  • 1. [Variants of radial hemimelia with and without vitium cordis (Holt-Oram syndrome) in 2 families].
    Pfeiffer RA; Böwing B; Deeg KH
    Monatsschr Kinderheilkd; 1989 May; 137(5):275-9. PubMed ID: 2739665
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [The Holt-Oram syndrome. Review of the literature and current orthopedic treatment concepts].
    Weber M; Wenz W; van Riel A; Kaufmann A; Graf J
    Z Orthop Ihre Grenzgeb; 1997; 135(4):368-75. PubMed ID: 9381776
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Variable clinical expression of Holt-Oram syndrome in three generations.
    Oğur G; Gül D; Lenk MK; Imirzalioğlu N; Alpay F; Oğur E
    Turk J Pediatr; 1998; 40(4):613-8. PubMed ID: 10028874
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phocomelia, flexion deformities and absent thumbs: a new hereditary upper limb malformation.
    Holmes LB; Borden S
    Pediatrics; 1974 Oct; 54(4):461-5. PubMed ID: 4415048
    [No Abstract]   [Full Text] [Related]  

  • 5. The upper limb-cardiovascular syndrome (Holt-Oram syndrome). A survey and a report of four cases.
    Sanz G; Nadal-Ginard B; Mata LA; Buentello L
    Clin Pediatr (Phila); 1973 Dec; 12(12):687-91 passim. PubMed ID: 4761183
    [No Abstract]   [Full Text] [Related]  

  • 6. Rare cardiac defect in Holt-Oram syndrome.
    Sinha R; Nema C
    Cardiovasc J Afr; 2012 Mar; 23(2):e3-4. PubMed ID: 22447508
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Variability of the Holt-Oram syndrome in Saudi individuals.
    Najjar H; Mardini M; Tabbaa R; Nyhan WL
    Am J Med Genet; 1988 Apr; 29(4):851-5. PubMed ID: 3400729
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Morphology and systematic aspects of the longitudinal radial defect].
    Martini AK
    Handchir Mikrochir Plast Chir; 1992 Jan; 24(1):16-22. PubMed ID: 1568670
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Holt-Oram syndrome associated with ectromelia and chromosomal aberrations.
    Rybak M; Kozlowski K; Kleczkowska A; Lewandowska J; Sokolowski J; Soltysik-Wilk E
    Am J Dis Child; 1971 Jun; 121(6):490-5. PubMed ID: 5581016
    [No Abstract]   [Full Text] [Related]  

  • 10. Variation in severity of cardiac disease in Holt-Oram syndrome.
    Sletten LJ; Pierpont ME
    Am J Med Genet; 1996 Oct; 65(2):128-32. PubMed ID: 8911604
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Holt-Oram syndrome: radiological approach.
    Penne D; Delanote G; Breysem L; Frijns JP; Smet MH; Baert AL
    J Belge Radiol; 1997 Jun; 80(3):118-9. PubMed ID: 9260393
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Limb anomalies in chromosomal aberrations.
    Pfeiffer RA; Santelmann R
    Birth Defects Orig Artic Ser; 1977; 13(1):319-37. PubMed ID: 322750
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hormonal versus genetic factors in limb and heart anomalies.
    el-Gindi E; Ahmed-Nasr M
    Cardiovasc Surg; 1993 Aug; 1(4):381-3. PubMed ID: 8076064
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome].
    Bonnet D; Terrett J; Pequignot-Viegas E; Weissenbach J; Munnich A; Lyonnet S; Kachaner J
    Arch Mal Coeur Vaiss; 1995 May; 88(5):661-6. PubMed ID: 7646274
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pathogenetic implications of muscular ventricular septal defect in Holt-Oram syndrome.
    Kumar A; Van Mierop LH; Epstein ML
    Am J Cardiol; 1994 May; 73(13):993-5. PubMed ID: 8184867
    [No Abstract]   [Full Text] [Related]  

  • 16. Holt-Oram syndrome: a clinical genetic study.
    Newbury-Ecob RA; Leanage R; Raeburn JA; Young ID
    J Med Genet; 1996 Apr; 33(4):300-7. PubMed ID: 8730285
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Diagnosis of familial Holt-Oram syndrome].
    Lehner R; Wenzl R; Vanura H; Frank W; Safar P; Husslein P
    Z Geburtshilfe Perinatol; 1994 Aug; 198(4):143-9. PubMed ID: 7975801
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Holt-Oram syndrome].
    Kullmann F; Grimm T
    Dtsch Med Wochenschr; 1993 Oct; 118(40):1455-62. PubMed ID: 8404501
    [No Abstract]   [Full Text] [Related]  

  • 19. [Holt-Oram syndrome and hand malformations associated with congenital heart disease].
    Pernot C; Dupuis C; Gilgenkrantz S; Hueber JM
    Arch Mal Coeur Vaiss; 1970 Oct; 63(10):1428-44. PubMed ID: 4993644
    [No Abstract]   [Full Text] [Related]  

  • 20. Genetic heterogeneity of heart-hand syndromes.
    Basson CT; Solomon SD; Weissman B; MacRae CA; Poznanski AK; Prieto F; Ruiz de la Fuente S; Pease WE; Levin SE; Holmes LB
    Circulation; 1995 Mar; 91(5):1326-9. PubMed ID: 7867169
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.