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Journal Abstract Search

91 related items for PubMed ID: 9211556

  • 1. Skeletal abnormalities in Meckel syndrome.
    Shanks J, Kerr B, Russell SA, Kingston H, Moore L.
    Pediatr Pathol Lab Med; 1997; 17(4):625-30. PubMed ID: 9211556
    [Abstract] [Full Text] [Related]

  • 2. Visceral anomalies in the Meckel syndrome.
    Rapola J, Salonen R.
    Teratology; 1985 Apr; 31(2):193-201. PubMed ID: 3992488
    [Abstract] [Full Text] [Related]

  • 3. Study of the malformation of ductal plate of the liver in Meckel syndrome and review of other syndromes presenting with this anomaly.
    Sergi C, Adam S, Kahl P, Otto HF.
    Pediatr Dev Pathol; 2000 Apr; 3(6):568-83. PubMed ID: 11000335
    [Abstract] [Full Text] [Related]

  • 4. Dandy-Walker malformation in the Meckel syndrome.
    Summers MC, Donnenfeld AE.
    Am J Med Genet; 1995 Jan 02; 55(1):57-61. PubMed ID: 7702098
    [Abstract] [Full Text] [Related]

  • 5. Cystic kidney dysplasia and polydactyly in 3 sibs with Bardet-Biedl syndrome.
    Gershoni-Baruch R, Nachlieli T, Leibo R, Degani S, Weissman I.
    Am J Med Genet; 1992 Oct 01; 44(3):269-73. PubMed ID: 1488972
    [Abstract] [Full Text] [Related]

  • 6. [Complex polydactyly of the limbs: mirror foot. Report of two cases and review of literature].
    Bonnet F, Garrido I, Haddad R, Pavy B, Mitrofanoff M.
    Ann Chir Plast Esthet; 2005 Aug 01; 50(4):323-7. PubMed ID: 16087041
    [Abstract] [Full Text] [Related]

  • 7. Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly".
    Fraser FC, Lytwyn A.
    Am J Med Genet; 1981 Aug 01; 9(1):67-73. PubMed ID: 7246621
    [Abstract] [Full Text] [Related]

  • 8. 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 Aug 01; 46(3):283-8. PubMed ID: 15503488
    [Abstract] [Full Text] [Related]

  • 9. The Meckel syndrome: clinicopathological findings in 67 patients.
    Salonen R.
    Am J Med Genet; 1984 Aug 01; 18(4):671-89. PubMed ID: 6486167
    [Abstract] [Full Text] [Related]

  • 10. Encephalocele, polycystic kidneys, and polydactyly as an autosomal recessive trait simulating certain other disorders: the Meckel syndrome.
    Mecke S, Passarge E.
    Ann Genet; 1971 Jun 01; 14(2):97-103. PubMed ID: 4997715
    [No Abstract] [Full Text] [Related]

  • 11. Meckel syndrome with Caroli disease and choledochal cysts.
    Venkatachala S, Sivaraman A.
    Fetal Pediatr Pathol; 2011 Jun 01; 30(5):350-4. PubMed ID: 21843058
    [Abstract] [Full Text] [Related]

  • 12. Meckel-Gruber syndrome. A lethal combination of abnormalities.
    Coard KC, Escoffery CT.
    West Indian Med J; 1990 Mar 01; 39(1):52-6. PubMed ID: 2333699
    [Abstract] [Full Text] [Related]

  • 13. Polydactyly, campomelia, ambiguous genitalia, cystic dysplastic kidneys, and cerebral malformation in a fetus of consanguineous parents: a new multiple malformation syndrome, or a severe form of oral-facial-digital syndrome type IV?
    Adès LC, Clapton WK, Morphett A, Morris LL, Haan EA.
    Am J Med Genet; 1994 Jan 15; 49(2):211-7. PubMed ID: 8116671
    [Abstract] [Full Text] [Related]

  • 14. Lack of cilia and differentiation defects in the liver of human foetuses with the Meckel syndrome.
    Clotman F, Libbrecht L, Killingsworth MC, Loo CC, Roskams T, Lemaigre FP.
    Liver Int; 2008 Mar 15; 28(3):377-84. PubMed ID: 17976156
    [Abstract] [Full Text] [Related]

  • 15. Anterior segment anomalies of the eye associated with multiple skeletal abnormalities and early lethality: confirmation of an autosomal recessive syndrome.
    al-Gazali LI, Bakir M, Sadaghatian MR, Nath R, Haas D.
    Clin Dysmorphol; 1999 Apr 15; 8(2):87-92. PubMed ID: 10319196
    [Abstract] [Full Text] [Related]

  • 16. Expanding the phenotypic spectrum of the Baller-Gerold syndrome.
    Temtamy SA, Aglan MS, Nemat A, Eid M.
    Genet Couns; 2003 Apr 15; 14(3):299-312. PubMed ID: 14577674
    [Abstract] [Full Text] [Related]

  • 17. Pathology of renal and hepatic anomalies in Meckel syndrome.
    Blankenberg TA, Ruebner BH, Ellis WG, Bernstein J, Dimmick JE.
    Am J Med Genet Suppl; 1987 Apr 15; 3():395-410. PubMed ID: 3130875
    [Abstract] [Full Text] [Related]

  • 18. Complex consanguinity associated with short rib-polydactyly syndrome III and congenital infection-like syndrome: a diagnostic problem in dysmorphic syndromes.
    al-Gazali LI, Sztriha L, Dawodu A, Varady E, Bakir M, Khdir A, Johansen J.
    J Med Genet; 1999 Jun 15; 36(6):461-6. PubMed ID: 10874634
    [Abstract] [Full Text] [Related]

  • 19. [Prenatal diagnosis of skeletal dysplasia: case report of a fetus with multiple anomalies].
    Novakov Mikić A, Stojić S, Konstantinidis G, Ristivojević A, Krnojelac D.
    Med Pregl; 2000 Jun 15; 53(3-4):197-201. PubMed ID: 10965689
    [Abstract] [Full Text] [Related]

  • 20. Meckel-Grüber syndrome: sonography and pathology.
    Ickowicz V, Eurin D, Maugey-Laulom B, Didier F, Garel C, Gubler MC, Laquerrière A, Avni EF.
    Ultrasound Obstet Gynecol; 2006 Mar 15; 27(3):296-300. PubMed ID: 16450359
    [Abstract] [Full Text] [Related]

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