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Journal Abstract Search

169 related items for PubMed ID: 15255329

  • 1. Meckel Gruber syndrome: occurrence in non-consanguineous marriages.
    de Silva MV, Senanayake H, Siriwardana KD.
    Ceylon Med J; 2004 Mar; 49(1):30-1. PubMed ID: 15255329
    [Abstract] [Full Text] [Related]

  • 2. Meckel Gruber syndrome--a single gene cause of recurrent neural tube defects.
    de Silva D, Suriyawansa D, Mangalika M, Samarasinghe D.
    Ceylon Med J; 2001 Mar; 46(1):30. PubMed ID: 11570001
    [Abstract] [Full Text] [Related]

  • 3. Meckel-Gruber syndrome.
    Ramachandran U, Malla T, Joshi KS.
    Kathmandu Univ Med J (KUMJ); 2006 Mar; 4(3):334-6. PubMed ID: 18603929
    [Abstract] [Full Text] [Related]

  • 4. Dandy-Walker malformation in the Meckel syndrome.
    Summers MC, Donnenfeld AE.
    Am J Med Genet; 1995 Jan 02; 55(1):57-61. PubMed ID: 7702098
    [Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis of Meckel-Gruber syndrome and Dandy-Walker malformation in four consecutive affected siblings, with the fourth one being diagnosed prenatally at 22 weeks of gestation.
    Balci S, Tekşen F, Dökmeci F, Cengiz B, Cömert RB, Can B, Ozdamar S.
    Turk J Pediatr; 2004 Jan 02; 46(3):283-8. PubMed ID: 15503488
    [Abstract] [Full Text] [Related]

  • 6. Phenotypic variability in Meckel-Gruber syndrome.
    Farag TI, Usha R, Uma R, Mady SA, al-Nagdy K, el-Badramany MH.
    Clin Genet; 1990 Sep 02; 38(3):176-9. PubMed ID: 2225527
    [Abstract] [Full Text] [Related]

  • 7. [Meckel-Gruber syndrome].
    Flessa A, Rempen A, Schmausser B, Marx A.
    Z Geburtshilfe Neonatol; 1996 Sep 02; 200(2):66-8. PubMed ID: 8767290
    [Abstract] [Full Text] [Related]

  • 8. Meckel Gruber syndrome.
    Anand JS, Javadekar BB, Belani MB.
    Indian Pediatr; 1988 Apr 02; 25(4):386-8. PubMed ID: 3225050
    [No Abstract] [Full Text] [Related]

  • 9. Meckel Gruber syndrome, A case report.
    Aslan K, Külahçı Aslan E, Orhan A, Atalay MA.
    Organogenesis; 2015 Apr 02; 11(2):87-92. PubMed ID: 26037304
    [Abstract] [Full Text] [Related]

  • 10. Phenotypic variation in Meckel syndrome.
    Seller MJ.
    Clin Genet; 1981 Jul 02; 20(1):74-7. PubMed ID: 7296953
    [Abstract] [Full Text] [Related]

  • 11. [Meckel syndrome. Update on a recurrent case].
    Calmelet P, Feidt X, Viville B, Olivier D, Treisser A.
    J Gynecol Obstet Biol Reprod (Paris); 1997 Jul 02; 26(4):435-41. PubMed ID: 9265071
    [Abstract] [Full Text] [Related]

  • 12. Polydactyly in a carrier of the gene for the Meckel syndrome.
    Nelson J, Nevin NC, Hanna EJ.
    Am J Med Genet; 1994 Nov 15; 53(3):207-9. PubMed ID: 7856653
    [Abstract] [Full Text] [Related]

  • 13. Meckel-Gruber syndrome. A lethal combination of abnormalities.
    Coard KC, Escoffery CT.
    West Indian Med J; 1990 Mar 15; 39(1):52-6. PubMed ID: 2333699
    [Abstract] [Full Text] [Related]

  • 14. Diagnosis of the Meckel-Gruber syndrome at eleven to fourteen weeks' gestation.
    Sepulveda W, Sebire NJ, Souka A, Snijders RJ, Nicolaides KH.
    Am J Obstet Gynecol; 1997 Feb 15; 176(2):316-9. PubMed ID: 9065174
    [Abstract] [Full Text] [Related]

  • 15. [2 new cases of Meckel-Gruber syndrome in the same family].
    Franzoni R, Scalercio A.
    Minerva Pediatr; 1986 Sep 30; 38(17-18):783-9. PubMed ID: 3796537
    [No Abstract] [Full Text] [Related]

  • 16. Genetic heterogeneity of Meckel syndrome.
    Roume J, Ma HW, Le Merrer M, Cormier-Daire V, Girlich D, Genin E, Munnich A.
    J Med Genet; 1997 Dec 30; 34(12):1003-6. PubMed ID: 9429143
    [Abstract] [Full Text] [Related]

  • 17. [Ultrasonic diagnosis of a hereditary multiple malformation syndrome: Meckel-Gruber syndrome or Carpenter-Hunter syndrome].
    Adjahoto EO, De Grandi P, Maillard-Brignon C, Pescia G.
    J Gynecol Obstet Biol Reprod (Paris); 1992 Dec 30; 21(8):928-33. PubMed ID: 1491139
    [Abstract] [Full Text] [Related]

  • 18. A review of Meckel-Gruber syndrome--incidence and outcome in the state of Qatar.
    Al-Belushi M, Al Ibrahim A, Ahmed M, Ahmed B, Khenyab N, Konje JC.
    J Matern Fetal Neonatal Med; 2016 Dec 30; 29(12):2013-6. PubMed ID: 26333300
    [Abstract] [Full Text] [Related]

  • 19. A prenatally diagnosed case of Meckel-Gruber syndrome with novel compound heterozygous pathogenic variants in the TXNDC15 gene.
    Ridnõi K, Šois M, Vaidla E, Pajusalu S, Kelder L, Reimand T, Õunap K.
    Mol Genet Genomic Med; 2019 May 30; 7(5):e614. PubMed ID: 30851085
    [Abstract] [Full Text] [Related]

  • 20. Meckel-Gruber syndrome: ultrasonographic and fetal autopsy correlation.
    Khurana S, Saini V, Wadhwa V, Kaur H.
    J Ultrasound; 2017 Jun 30; 20(2):167-170. PubMed ID: 28593008
    [Abstract] [Full Text] [Related]

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