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 *

100 related articles for article (PubMed ID: 11897819)

  • 1. 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]  

  • 2. 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]  

  • 3. [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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Familial occurrence of the Wiedemann-Beckwith syndrome and persistent fontanel.
    Sommer A; Cutler EA; Cohen BL; Harper D; Backes C
    Am J Med Genet; 1977; 1(1):59-63. PubMed ID: 610426
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. [Asymptomatic familial basal ganglia calcification with autosomal dominant inheritance: a family report].
    Yamada N; Hayashi T
    No To Hattatsu; 2000 Nov; 32(6):515-9. PubMed ID: 11144166
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A familial syndromal form of omphalocele.
    Port-Lis M; Leroy C; Manouvrier S; Escande F; Passemard S; Perrin L; Capri Y; Gérard B; Verloes A
    Eur J Med Genet; 2011; 54(3):337-40. PubMed ID: 21333766
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characteristics and outcome of 90 cases of fetal omphalocele.
    Brantberg A; Blaas HG; Haugen SE; Eik-Nes SH
    Ultrasound Obstet Gynecol; 2005 Oct; 26(5):527-37. PubMed ID: 16184512
    [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. Familial hiatal hernia in a large five generation family confirming true autosomal dominant inheritance.
    Carré IJ; Johnston BT; Thomas PS; Morrison PJ
    Gut; 1999 Nov; 45(5):649-52. PubMed ID: 10517898
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Four cases of omphalocele in two generations of the same family.
    Osuna A; Lindham S
    Clin Genet; 1976 Mar; 9(3):354-6. PubMed ID: 131012
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. 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]  

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

  • 19. Autosomal dominant inheritance of tibial meromelia. Report of a kindred.
    Clark MW
    J Bone Joint Surg Am; 1975 Mar; 57(2):262-4. PubMed ID: 1112852
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Shprintzen-Goldberg omphalocele syndrome: a new patient with an expanded phenotype.
    Zelante L; Germano M; Sacco M; Calvano S
    Am J Med Genet A; 2006 Feb; 140(4):383-4. PubMed ID: 16411191
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.