BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 5115888)

  • 1. Exomphalos in four consecutive pregnancies.
    Kucera J; Goetz P
    Humangenetik; 1971; 13(1):58-60. PubMed ID: 5115888
    [No Abstract]   [Full Text] [Related]  

  • 2. Exomphalos and trisomy 18 syndrome. Report of two cases.
    Zizka J; Balícek P; Pokorná E; Dostalíková K; Kodousková M
    Hum Genet; 1976 May; 32(2):221-3. PubMed ID: 1270082
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?
    Donnai D; Barrow M
    Am J Med Genet; 1993 Oct; 47(5):679-82. PubMed ID: 8266995
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The outcomes of pregnancies following a prenatal diagnosis of fetal exomphalos in Western Australia.
    Calvert N; Damiani S; Sunario J; Bower C; Dickinson JE
    Aust N Z J Obstet Gynaecol; 2009 Aug; 49(4):371-5. PubMed ID: 19694690
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Exomphalos-macroglossia-gigantism syndrome].
    Mücke J
    Kinderarztl Prax; 1972 Jan; 40(1):10-4. PubMed ID: 5017807
    [No Abstract]   [Full Text] [Related]  

  • 6. Lethal multiple pterygium syndrome associated with omphalocele.
    Chen CP
    Genet Couns; 2007; 18(4):451-3. PubMed ID: 18286827
    [No Abstract]   [Full Text] [Related]  

  • 7. Heterogeneity in omphalocoele with absent radial ray complex.
    Devriendt K; Fryns JP; Moerman P; Vanhole C; Devlieger H
    Am J Med Genet; 1999 Jan; 82(1):95-6. PubMed ID: 9916853
    [No Abstract]   [Full Text] [Related]  

  • 8. Prenatal diagnosis of omphalocele associated with umbilical cord cyst.
    Chen CP; Jan SW; Liu FF; Chiang S; Huang SH; Sheu JC; Wang KG; Lan CC
    Acta Obstet Gynecol Scand; 1995 Nov; 74(10):832-5. PubMed ID: 8533570
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Definitive surgical management of antenatally diagnosed exomphalos.
    Rijhwani A; Davenport M; Dawrant M; Dimitriou G; Patel S; Greenough A; Nicolaides K
    J Pediatr Surg; 2005 Mar; 40(3):516-22. PubMed ID: 15793728
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Impact of antenatal diagnosis on incidence and prognosis in abdominal wall defects.
    Fisher R; Attah A; Partington A; Dykes E
    J Pediatr Surg; 1996 Apr; 31(4):538-41. PubMed ID: 8801308
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [EMG syndrome. Review apropo of 2 cases].
    Torres V; Torres CC
    Med Cutan Ibero Lat Am; 1977; 5(1):53-8. PubMed ID: 561276
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Donnai-Barrow syndrome: four additional patients.
    Chassaing N; Lacombe D; Carles D; Calvas P; Saura R; Bieth E
    Am J Med Genet A; 2003 Sep; 121A(3):258-62. PubMed ID: 12923867
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diaphragmatic hernia-exomphalos-hypertelorism syndrome: a new case and further evidence of autosomal recessive inheritance.
    Gripp KW; Donnai D; Clericuzio CL; McDonald-McGinn DM; Guttenberg M; Zackai EH
    Am J Med Genet; 1997 Feb; 68(4):441-4. PubMed ID: 9021018
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Current outcome of antenatally diagnosed exomphalos: an 11 year review.
    Lakasing L; Cicero S; Davenport M; Patel S; Nicolaides KH
    J Pediatr Surg; 2006 Aug; 41(8):1403-6. PubMed ID: 16863845
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The "E.M.G." syndrome (Exomphalos, Macroglossia, Gigantism).
    Irving IM
    Prog Pediatr Surg; 1970; 1():1-61. PubMed ID: 4942287
    [No Abstract]   [Full Text] [Related]  

  • 16. Fetal omphalocele: associated malformations and chromosomal defects.
    Gilbert WM; Nicolaides KH
    Obstet Gynecol; 1987 Oct; 70(4):633-5. PubMed ID: 3306512
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new lethal syndrome of exomphalos, short limbs, and macrogonadism.
    Faivre L; Delezoide AL; Narcy F; Razavi F; Bouvier R; Cormier-Daire V; Briard ML; Lyonnet S; Vekemans M; Munnich A; Le Merrer M
    J Med Genet; 1999 Feb; 36(2):131-6. PubMed ID: 10051012
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Malpuech syndrome: a possible relationship with the Wolf-Hirschhorn/Pitt-Roger-Danks phenotype.
    Selicorni A; Faravelli F
    Am J Med Genet; 2000 Nov; 95(3):291. PubMed ID: 11102941
    [No Abstract]   [Full Text] [Related]  

  • 19. Abnormal karyotype of fetuses with omphalocele: prediction based on omphalocele contents.
    Benacerraf BR; Saltzman DH; Estroff JA; Frigoletto FD
    Obstet Gynecol; 1990 Mar; 75(3 Pt 1):317-9. PubMed ID: 2304703
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rieger syndrome with exomphalos.
    Reddihough DS; Rogers JG; Keith CG
    Aust Paediatr J; 1982 Jun; 18(2):130-1. PubMed ID: 6814412
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.