189 related articles for article (PubMed ID: 11570001)
1. 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
[TBL] [Abstract][Full Text] [Related]
2. 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
[TBL] [Abstract][Full Text] [Related]
3. 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; 46(3):283-8. PubMed ID: 15503488
[TBL] [Abstract][Full Text] [Related]
4. [The Meckel syndrome (author's transl)].
Leucht W; Heyes H; Müller E; Schmidt W
Geburtshilfe Frauenheilkd; 1981 Nov; 41(11):765-8. PubMed ID: 6172316
[TBL] [Abstract][Full Text] [Related]
5. Meckel-Gruber syndrome. A lethal combination of abnormalities.
Coard KC; Escoffery CT
West Indian Med J; 1990 Mar; 39(1):52-6. PubMed ID: 2333699
[TBL] [Abstract][Full Text] [Related]
6. Meckel-Gruber syndrome.
Ramachandran U; Malla T; Joshi KS
Kathmandu Univ Med J (KUMJ); 2006; 4(3):334-6. PubMed ID: 18603929
[TBL] [Abstract][Full Text] [Related]
7. Meckel-Gruber syndrome: ultrasonographic and fetal autopsy correlation.
Khurana S; Saini V; Wadhwa V; Kaur H
J Ultrasound; 2017 Jun; 20(2):167-170. PubMed ID: 28593008
[TBL] [Abstract][Full Text] [Related]
8. [Meckel syndrome. Update on a recurrent case].
Calmelet P; Feidt X; Viville B; Olivier D; Treisser A
J Gynecol Obstet Biol Reprod (Paris); 1997; 26(4):435-41. PubMed ID: 9265071
[TBL] [Abstract][Full Text] [Related]
9. Meckel Gruber syndrome, A case report.
Aslan K; Külahçı Aslan E; Orhan A; Atalay MA
Organogenesis; 2015; 11(2):87-92. PubMed ID: 26037304
[TBL] [Abstract][Full Text] [Related]
10. Phenotypic variability in Meckel-Gruber syndrome.
Farag TI; Usha R; Uma R; Mady SA; al-Nagdy K; el-Badramany MH
Clin Genet; 1990 Sep; 38(3):176-9. PubMed ID: 2225527
[TBL] [Abstract][Full Text] [Related]
11. Dandy-Walker malformation in the Meckel syndrome.
Summers MC; Donnenfeld AE
Am J Med Genet; 1995 Jan; 55(1):57-61. PubMed ID: 7702098
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of Meckel-Gruber syndrome case reports.
Su SL; Liu CM; Lee JN
Gaoxiong Yi Xue Ke Xue Za Zhi; 1995 Feb; 11(2):127-32. PubMed ID: 7707455
[TBL] [Abstract][Full Text] [Related]
13. Meckel syndrome: genetics, perinatal findings, and differential diagnosis.
Chen CP
Taiwan J Obstet Gynecol; 2007 Mar; 46(1):9-14. PubMed ID: 17389183
[TBL] [Abstract][Full Text] [Related]
14. [Meckel-Gruber syndrome].
Flessa A; Rempen A; Schmausser B; Marx A
Z Geburtshilfe Neonatol; 1996; 200(2):66-8. PubMed ID: 8767290
[TBL] [Abstract][Full Text] [Related]
15. Meckel-Gruber syndrome.
Gazioğlu N; Vural M; Seçkin MS; Tüysüz B; Akpir E; Kuday C; Ilikkan B; Erginel A; Cenani A
Childs Nerv Syst; 1998 Mar; 14(3):142-5. PubMed ID: 9579873
[TBL] [Abstract][Full Text] [Related]
16. 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
[TBL] [Abstract][Full Text] [Related]
17. 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; 7(5):e614. PubMed ID: 30851085
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of Meckel syndrome.
Fryns JP; Vandenberghe K; Van Assche FA; Cassiman JJ; van den Berghe H
J Genet Hum; 1980 Dec; 28(4):89-94. PubMed ID: 7205201
[TBL] [Abstract][Full Text] [Related]
19. Phenotypic variation in Meckel syndrome.
Seller MJ
Clin Genet; 1981 Jul; 20(1):74-7. PubMed ID: 7296953
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of Meckel Gruber syndrome presenting with renal agenesis: report of a case.
Guven MA; Ceylaner S; Ceylaner G; Gul D; Ertas IE
Genet Couns; 2006; 17(1):65-8. PubMed ID: 16719279
[No Abstract] [Full Text] [Related]
[Next] [New Search]