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 *

128 related articles for article (PubMed ID: 7172476)

  • 1. Ivemark syndrome in siblings.
    Hurwitz RC; Caskey CT
    Clin Genet; 1982 Jul; 22(1):7-11. PubMed ID: 7172476
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family.
    Arnold GL; Bixler D; Girod D
    Am J Med Genet; 1983 Sep; 16(1):35-42. PubMed ID: 6638068
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Familial heterotaxy syndrome. Case report and review of the international literature].
    Cesko I; Hajdú J; Marton T; Tarnai L; Zs Tóth E
    Orv Hetil; 1998 Nov; 139(46):2775-8. PubMed ID: 9849063
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Simultaneous occurrence of Ivemark syndrome and diprosopus].
    Jójárt G
    Orv Hetil; 1980 Dec; 121(50):3095. PubMed ID: 7220027
    [No Abstract]   [Full Text] [Related]  

  • 5. Ivemark syndrome with asplenia in siblings.
    Cesko I; Hajdú J; Tóth T; Marton T; Papp C; Papp Z
    J Pediatr; 1997 May; 130(5):822-4. PubMed ID: 9152295
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial occurrence of Ivemark syndrome with splenic hypoplasia and asplenia in sibs.
    Simpson J; Zellweger H
    J Med Genet; 1973 Sep; 10(3):303-4. PubMed ID: 4774542
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Does Ser364Pro mutation of connexin 43 exist in Taiwanese patients with Ivemark syndrome?
    Chen WC; Tsai FJ; Wu JY; Wu HC; Li CW
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Sep; 63(9):691-5. PubMed ID: 11037645
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Ivemark syndrome: 2 case reports].
    Roth P; Agnani G; Arbez-Gindre F; Roux C; Martin A; Colette C
    J Gynecol Obstet Biol Reprod (Paris); 1993; 22(7):771-5. PubMed ID: 8308205
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial situs inversus and congenital heart defects.
    Zlotogora J; Schimmel MS; Glaser Y
    Am J Med Genet; 1987 Jan; 26(1):181-4. PubMed ID: 3812559
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of Meckel syndrome with M-anisosplenia in one patient.
    Moerman P; Verbeken E; Fryns JP; Goddeeris P; Lauweryns JM
    Clin Genet; 1982 Sep; 22(3):143-7. PubMed ID: 7151299
    [No Abstract]   [Full Text] [Related]  

  • 11. Dextrocardia with situs inversus and isolated levocardia in two male siblings.
    Nair KV
    Indian Heart J; 1972 Jul; 24(3):300-4. PubMed ID: 4658677
    [No Abstract]   [Full Text] [Related]  

  • 12. X-linked laterality sequence: situs inversus, complex cardiac defects, splenic defects.
    Mathias RS; Lacro RV; Jones KL
    Am J Med Genet; 1987 Sep; 28(1):111-6. PubMed ID: 3674105
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Asplenia syndrome(Ivemark syndrome)].
    Yamaguchi M; Oshima Y
    Ryoikibetsu Shokogun Shirizu; 2000; (32):305-7. PubMed ID: 11212725
    [No Abstract]   [Full Text] [Related]  

  • 14. [An unusual form of Ivemark syndrome].
    Szendröi M; Egerváry M
    Orv Hetil; 1982 Oct; 123(44):2725-7. PubMed ID: 7145434
    [No Abstract]   [Full Text] [Related]  

  • 15. [On a case of Ivemark's syndrome].
    Alfieri A; Malgarini F
    Policlinico Prat; 1967 May; 74(22):734-8. PubMed ID: 5611156
    [No Abstract]   [Full Text] [Related]  

  • 16. Spina bifida and so-called asplenia syndrome occurring separately in sibs.
    Van Went JJ; Van Went GF; Delleman JW; Becker AG
    Teratology; 1977 Apr; 15(2):195-8. PubMed ID: 325678
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ivemark syndrome with agenesis of the corpus callosum: a case report with a review of the literature.
    Noack F; Sayk F; Ressel A; Berg C; Gembruch U; Reusche E
    Prenat Diagn; 2002 Nov; 22(11):1011-5. PubMed ID: 12424766
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Risk factors for situs defects and congenital heart disease in primary ciliary dyskinesia.
    Best S; Shoemark A; Rubbo B; Patel MP; Fassad MR; Dixon M; Rogers AV; Hirst RA; Rutman A; Ollosson S; Jackson CL; Goggin P; Thomas S; Pengelly R; Cullup T; Pissaridou E; Hayward J; Onoufriadis A; O'Callaghan C; Loebinger MR; Wilson R; Chung EM; Kenia P; Doughty VL; Carvalho JS; Lucas JS; Mitchison HM; Hogg C
    Thorax; 2019 Feb; 74(2):203-205. PubMed ID: 30166424
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gouty arthritis in a patient with Ivemark syndrome.
    Bhattacharjee M; Friedman AW; Thiagarajan P
    South Med J; 1996 Aug; 89(8):834-5. PubMed ID: 8701391
    [No Abstract]   [Full Text] [Related]  

  • 20. [Complex congenital heart diseases, situs inversus and splenic agenesis (Ivemark syndrome)].
    FONTAN A; VERGER P; BATTIN JJ; ALBERTY
    Arch Fr Pediatr; 1962 Jan; 19():107-14. PubMed ID: 13893942
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.