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 *

153 related articles for article (PubMed ID: 8946132)

  • 21. Deciphering the molecular genetics of congenital heart disease.
    Bouvagnet P; Sauer U; Debrus S; Genz T; Alonso S; Berger G; De Meeus A; Bühlmeier K; Demaille J
    Herz; 1994 Apr; 19(2):119-25. PubMed ID: 8194832
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetic counseling in congenital heart disease.
    Nora JJ
    Adv Cardiol; 1974; 11(00):56-66. PubMed ID: 4413561
    [No Abstract]   [Full Text] [Related]  

  • 23. Heritable syndromes with skeletal abnormalities and congenital heart disease.
    Martin EC
    N Y State J Med; 1977 May; 77(6):944-50. PubMed ID: 140338
    [No Abstract]   [Full Text] [Related]  

  • 24. [49,XXXXY syndrome and congenital cardiopathy].
    Darwiche A; Lusson JR; Marcaggi X; Labbe A
    Arch Fr Pediatr; 1991 May; 48(5):376. PubMed ID: 1859248
    [No Abstract]   [Full Text] [Related]  

  • 25. A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12.
    Bonnet D; Pelet A; Legeai-Mallet L; Sidi D; Mathieu M; Parent P; Plauchu H; Serville F; Schinzel A; Weissenbach J
    Nat Genet; 1994 Apr; 6(4):405-8. PubMed ID: 8054983
    [TBL] [Abstract][Full Text] [Related]  

  • 26. TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts.
    Reamon-Buettner SM; Borlak J
    Hum Mutat; 2004 Jul; 24(1):104. PubMed ID: 15221798
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery.
    Ziolkowska L; Kawalec W; Turska-Kmiec A; Krajewska-Walasek M; Brzezinska-Rajszys G; Daszkowska J; Maruszewski B; Burczynski P
    Eur J Pediatr; 2008 Oct; 167(10):1135-40. PubMed ID: 18172682
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2].
    Trost D; Engels H; Bauriedel G; Wiebe W; Schwanitz G
    Dtsch Med Wochenschr; 1999 Jan; 124(1-2):3-7. PubMed ID: 9951451
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Absent Left Main Coronary Artery and Separate Ostia of Left Coronary System in a Patient with Holt-Oram Syndrome and Sinus Node Dysfunction.
    Aung TT; Roberto ES; Wase A
    Am J Case Rep; 2016 Feb; 17():93-6. PubMed ID: 26882979
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Holt-Oram syndrome revisited. Two patients in the same family.
    Frota Filho JD; Pereira W; Leiria TL; Vallenas M; Leães PE; Blacher C; Lúcio E; Lucchese FA
    Arq Bras Cardiol; 1999 Nov; 73(5):429-34. PubMed ID: 10887363
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. A case of chromosome abnormality (46, XX, Gq+) with congenital heart disease and leprechaunism.
    Iwaski H; Abe M; Nawate G; Kato H
    Jinrui Idengaku Zasshi; 1974 Jun; 19(1):82-3. PubMed ID: 4476865
    [No Abstract]   [Full Text] [Related]  

  • 33. [Fetal echocardiography and clinical genetics--a close correlation].
    Zerres K; Gembruch U; Schwanitz G; Redel DA; Bald R; Gottschlich A; Hansmann M
    Z Kardiol; 1990 Feb; 79(2):96-106. PubMed ID: 2321416
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Holt-Oram syndrome: a case report.
    Chin J; Pereira S; Camacho A; Pessoa B; Bento D; Amado J; Pereira J; de Jesus I
    Rev Port Cardiol; 2014 Nov; 33(11):737.e1-5. PubMed ID: 25455949
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Holt-Oram syndrome with chromosomopathy (author's transl)].
    González Espinosa C; Artiles Pérez L; García Báez M; Otero Gómez A; García Miranda JL
    An Esp Pediatr; 1982 Jan; 16(1):77-81. PubMed ID: 7081854
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome).
    Basson CT; Cowley GS; Solomon SD; Weissman B; Poznanski AK; Traill TA; Seidman JG; Seidman CE
    N Engl J Med; 1994 Mar; 330(13):885-91. PubMed ID: 8114858
    [TBL] [Abstract][Full Text] [Related]  

  • 37. BMPR2 mutations in pulmonary arterial hypertension with congenital heart disease.
    Roberts KE; McElroy JJ; Wong WP; Yen E; Widlitz A; Barst RJ; Knowles JA; Morse JH
    Eur Respir J; 2004 Sep; 24(3):371-4. PubMed ID: 15358693
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [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]  

  • 39. Surgical experience with congenital heart disease in Down's syndrome.
    Parvathy U; Balakrishnan KR; Ranjith MS; Saldanha R; Sai S; Vakamudi M
    Indian Heart J; 2000; 52(4):438-41. PubMed ID: 11084787
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Interstitial deletion of chromosome 5 in a neonate due to maternal insertion, ins(8;5)(p23;q33q35).
    Gibbons B; Tan SY; Kee SK; Quaife R; Lim ST
    Am J Med Genet; 1999 Sep; 86(3):289-93. PubMed ID: 10482883
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.