These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

73 related articles for article (PubMed ID: 5559527)

  • 1. [Unusual case of familial incidence of omphalocele].
    Kucera J; Goetz P; Antalík J
    Cesk Pediatr; 1971 May; 26(5):237-9. PubMed ID: 5559527
    [No Abstract]   [Full Text] [Related]  

  • 2. Familial omphalocele and recurrence risk.
    Lurie IW; Ilyina HG
    Am J Med Genet; 1984 Feb; 17(2):541-3. PubMed ID: 6702903
    [No Abstract]   [Full Text] [Related]  

  • 3. Familial omphalocele: analysis of risk factors and case report.
    DiLiberti JH
    Am J Med Genet; 1982 Nov; 13(3):263-8. PubMed ID: 7180872
    [No Abstract]   [Full Text] [Related]  

  • 4. [Omphalocele: hereditary disease with dominant transmission?].
    Le Marec B; Roussey M; Bracq H; Babut JM
    J Genet Hum; 1979 Oct; 27(3):259-62. PubMed ID: 536741
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial occurrence of omphalocele.
    Rott HD; Truckenbrodt H
    Humangenetik; 1974; 24(3):259-60. PubMed ID: 4442871
    [No Abstract]   [Full Text] [Related]  

  • 6. Familial omphalocele: considerations in genetic counseling.
    Pryde PG; Greb A; Isada NB; Johnson MB; Klein M; Evans MI
    Am J Med Genet; 1992 Nov; 44(5):624-7. PubMed ID: 1481822
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial omphalocele.
    Steele K; Nevin NC
    Ulster Med J; 1985 Oct; 54(2):214-5. PubMed ID: 4095814
    [No Abstract]   [Full Text] [Related]  

  • 8. [Wiedemann and Beckwith syndrome: a new familial case].
    Piussan C; Risbourg B; Lenaerts C; Delvallez N; Gontier MF; Vitse M
    J Genet Hum; 1980 Sep; 28(3):281-91. PubMed ID: 7463028
    [No Abstract]   [Full Text] [Related]  

  • 9. Familial occurrence of omphalocele suggesting sex-linked inheritance.
    Havalad S; Noblett H; Speidel BD
    Arch Dis Child; 1979 Feb; 54(2):142-3. PubMed ID: 434891
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Editorial comment on the letter by Lurie and Ilyina on familial omphalocele.
    Baird PA
    Am J Med Genet; 1984 Feb; 17(2):545. PubMed ID: 6702904
    [No Abstract]   [Full Text] [Related]  

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

  • 12. [Gastroschisis and omphalocele in the same family (author's transl)].
    Gaillard D
    Arch Fr Pediatr; 1980 Oct; 37(8):537-8. PubMed ID: 6449916
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dysmorphic facies, omphalocele, laryngeal and pharyngeal hypoplasia, spinal anomalies, and learning disabilities in a new dominant malformation syndrome.
    Shprintzen RJ; Goldberg RB
    Birth Defects Orig Artic Ser; 1979; 15(5B):347-53. PubMed ID: 526588
    [No Abstract]   [Full Text] [Related]  

  • 14. Otopalatodigital syndrome type II associated with omphalocele: report of three cases.
    Young K; Barth CK; Moore C; Weaver DD
    Am J Med Genet; 1993 Feb; 45(4):481-7. PubMed ID: 8465856
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Omphalocele and multiple severe congenital anomalies associated with osteodysplasty (Melnick-Needles syndrome).
    von Oeyen P; Holmes LB; Trelstad RL; Griscom NT
    Am J Med Genet; 1982 Dec; 13(4):453-63. PubMed ID: 7158644
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family.
    Best LG; Hoekstra RE
    Am J Med Genet; 1981; 9(4):291-9. PubMed ID: 7294068
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Omphalocele and gastroschisis: a collaborative study of five Italian congenital malformation registries.
    Calzolari E; Volpato S; Bianchi F; Cianciulli D; Tenconi R; Clementi M; Calabro A; Lungarotti S; Mastroiacovo PP; Botto L
    Teratology; 1993 Jan; 47(1):47-55. PubMed ID: 8475457
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Omphalocele in three generations with autosomal dominant transmission.
    Kanagawa SL; Begleiter ML; Ostlie DJ; Holcomb G; Drake W; Butler MG
    J Med Genet; 2002 Mar; 39(3):184-5. PubMed ID: 11897819
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Omphalocele in half-siblings.
    Kapur S; Higgins JV; Scott-Emuakpor AB; Dolanski EA
    Clin Genet; 1980 Jul; 18(1):88-90. PubMed ID: 7418258
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The changing face of gastroschisis and omphalocele in southeast Georgia.
    Goldkrand JW; Causey TN; Hull EE
    J Matern Fetal Neonatal Med; 2004 May; 15(5):331-5. PubMed ID: 15280125
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.