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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]
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]
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]