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216 related items for PubMed ID: 26037304
1. Meckel Gruber syndrome, A case report. Aslan K, Külahçı Aslan E, Orhan A, Atalay MA. Organogenesis; 2015; 11(2):87-92. PubMed ID: 26037304 [Abstract] [Full Text] [Related]
3. 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 Jun; 29(12):2013-6. PubMed ID: 26333300 [Abstract] [Full Text] [Related]
4. 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; 176(2):316-9. PubMed ID: 9065174 [Abstract] [Full Text] [Related]
5. [Meckel Gruber syndrome: about a rare case]. Itchimouh S, Khabtou K, Mahdaoui S, Boufettal H, Samouh N. Pan Afr Med J; 2016 Feb; 25():43. PubMed ID: 28154732 [Abstract] [Full Text] [Related]
6. Meckel-Gruber Syndrome: A Case Who Lived for 5 Months. Aydin Ozturk P, Asena M, Katar S, Ozturk U. Pediatr Neurosurg; 2019 Feb; 54(4):277-280. PubMed ID: 31261150 [Abstract] [Full Text] [Related]
7. First-trimester diagnosis of Meckel-Gruber syndrome by fetal ultrasound with molecular identification of CC2D2A mutations by next-generation sequencing. Jones D, Fiozzo F, Waters B, McKnight D, Brown S. Ultrasound Obstet Gynecol; 2014 Dec; 44(6):719-21. PubMed ID: 24706459 [Abstract] [Full Text] [Related]
10. Prenatal diagnosis of Meckel-Gruber syndrome in a pregnancy obtained with ICSI. Celentano C, Prefumo F, Liberati M, Gallo G, Di Nisio Q, Rotmensch S. J Assist Reprod Genet; 2006 Jun 01; 23(6):281-3. PubMed ID: 16832598 [Abstract] [Full Text] [Related]
11. Meckel-Gruber syndrome: a rare clinical entity. Jha T, Bardhan J, Das B, Patra KK, Dhali B, Seth S. J Indian Med Assoc; 2010 Sep 01; 108(9):611-2. PubMed ID: 21510539 [Abstract] [Full Text] [Related]
12. Earliest ultrasound findings and description of splicing mutations in Meckel-Gruber syndrome. Eckmann-Scholz C, Jonat W, Zerres K, Ortiz-Brüchle N. Arch Gynecol Obstet; 2012 Oct 01; 286(4):917-21. PubMed ID: 22699515 [Abstract] [Full Text] [Related]
13. 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 01; 7(5):e614. PubMed ID: 30851085 [Abstract] [Full Text] [Related]
14. Meckel-Gruber syndrome together with Dandy-Walker malformation: an atypical case report of a 2nd recurrence in a consanguine marriage. Alsamal M, Zitoun OA, Abdulghani EA, Sula I. Childs Nerv Syst; 2024 Jan 01; 40(1):257-261. PubMed ID: 37530877 [Abstract] [Full Text] [Related]
15. 12q21 Microdeletion in a fetus with Meckel syndrome involving CEP290/MKS4. Molin A, Benoist G, Jeanne-Pasquier C, Elkartoufi N, Litzer J, Decamp M, Gruchy N, Durand-Malbruny M, Begorre M, Attie-Bitach T, Leporrier N. Eur J Med Genet; 2013 Oct 01; 56(10):580-3. PubMed ID: 23954617 [Abstract] [Full Text] [Related]
16. Antenatal diagnosis of left atrial isomerism and heterotaxy syndrome in fetus with Meckel-Gruber syndrome. Kurtulmuş S, Demirpençe S, Can Öztekin D, Koç A, Tavlı V. Turk Kardiyol Dern Ars; 2014 Mar 01; 42(2):182-5. PubMed ID: 24643152 [Abstract] [Full Text] [Related]
17. 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 01; 46(1):30. PubMed ID: 11570001 [Abstract] [Full Text] [Related]
18. Early prenatal diagnosis of Meckel syndrome--a case report. Yu CJ, Chen CP, Jeng CJ, Yang YC. Zhonghua Yi Xue Za Zhi (Taipei); 1990 Jul 01; 46(1):53-6. PubMed ID: 2176925 [Abstract] [Full Text] [Related]
19. [Ultrasound diagnosis of Meckel-Gruber syndrome at 13 weeks of gestation in families at risk--a case report and literature review]. Mazneŭkova V, Kamenov E, Dimitrova L. Akush Ginekol (Sofiia); 2002 Jul 01; 41(5):42-5. PubMed ID: 12440339 [Abstract] [Full Text] [Related]
20. Uniparental disomy as an unexpected cause of Meckel-Gruber syndrome: report of a case. Bruechle NO, Steuernagel P, Zerres K, Kurth I, Eggermann T, Knopp C. Pediatr Nephrol; 2017 Oct 01; 32(10):1989-1992. PubMed ID: 28620746 [Abstract] [Full Text] [Related] Page: [Next] [New Search]