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Journal Abstract Search

110 related items for PubMed ID: 8055140

  • 1. Prenatal ultrasound findings in a fetus with otopalatodigital syndrome type II.
    Eccles DM, Moore IE, Cook S, Griffin DR, Chitty L, Hall CM, Temple IK.
    Clin Dysmorphol; 1994 Apr; 3(2):175-9. PubMed ID: 8055140
    [Abstract] [Full Text] [Related]

  • 2. Twin fetuses with abnormalities that overlap with three midline malformation complexes.
    Hingorani SR, Pagon RA, Shepard TH, Kapur RP.
    Am J Med Genet; 1991 Nov 01; 41(2):230-5. PubMed ID: 1785640
    [Abstract] [Full Text] [Related]

  • 3. On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant gene.
    Alembik Y, Stoll C, Messer J.
    Genet Couns; 1997 Nov 01; 8(2):133-7. PubMed ID: 9219012
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 45(4):481-7. PubMed ID: 8465856
    [Abstract] [Full Text] [Related]

  • 5. The caudal regression syndrome in infants of diabetic mothers.
    Perrot LJ, Williamson S, Jimenez JF.
    Ann Clin Lab Sci; 1987 Feb 15; 17(4):211-20. PubMed ID: 3304122
    [Abstract] [Full Text] [Related]

  • 6. Atelosteogenesis type I: autopsy findings.
    Wessels A, Wainwright HC, Beighton P.
    Pediatr Dev Pathol; 2011 Feb 15; 14(6):496-500. PubMed ID: 21985323
    [Abstract] [Full Text] [Related]

  • 7. Early fetal akinesia deformation sequence: a case report with unusual autoptic features.
    Giordano G, Gnetti L, Froio E, Ricci R.
    J Matern Fetal Neonatal Med; 2005 May 15; 17(5):349-52. PubMed ID: 16147849
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of a Turkish Bartsocas-Papas syndrome case with upper limb pterigia.
    Ceylaner G, Güven MA, Ceylaner S, Uzel M, Müftüoğlu K.
    Prenat Diagn; 2007 Jun 15; 27(6):563-5. PubMed ID: 17457955
    [Abstract] [Full Text] [Related]

  • 9. Multiple congenital anomalies associated with an oto-palato-digital syndrome type II.
    Blanchet P, Lefort G, Eglin MC, Rieu D, Sarda P.
    Genet Couns; 1993 Jun 15; 4(4):289-94. PubMed ID: 8110417
    [Abstract] [Full Text] [Related]

  • 10. Second-trimester diagnosis of limb-body wall complex with literature review of pathogenesis.
    Chen CP, Lin CJ, Chang TY, Hsu CY, Tzen CY, Wang W.
    Genet Couns; 2007 Jun 15; 18(1):105-12. PubMed ID: 17515306
    [Abstract] [Full Text] [Related]

  • 11. Early prenatal diagnosis of polycystic pancreas with narrow thorax and short limb dwarfism.
    Bronstein M, Reichler A, Borochowitz Z, Bejar J, Drugan A.
    Am J Med Genet; 1994 Jan 01; 49(1):6-9. PubMed ID: 8172252
    [Abstract] [Full Text] [Related]

  • 12. Antenatally diagnosed thanatophoric dysplasia.
    Tóth Z, Vachter J, Szeifert G, Nemes Z, Csécsei K, Török O, Harsányi A, Papp Z.
    Acta Paediatr Acad Sci Hung; 1982 Jan 01; 23(4):423-30. PubMed ID: 6763446
    [Abstract] [Full Text] [Related]

  • 13. Midtrimester prenatal diagnosis of short-limb dwarfism (Saldino-Noonan syndrome).
    Johnson VP, Petersen LP, Holzwarth DR, Messner FD.
    Birth Defects Orig Artic Ser; 1982 Jan 01; 18(3 Pt A):133-41. PubMed ID: 7126786
    [No Abstract] [Full Text] [Related]

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  • 15. Oto-palato-digital syndrome with features of type I and II in brothers.
    Horn D, Nitz I, Bollmann R.
    Genet Couns; 1995 Jan 01; 6(3):233-40. PubMed ID: 8588852
    [Abstract] [Full Text] [Related]

  • 16. Vascular abnormalities in a fetus with multiple pterygia.
    Fitch N, Rochon L, Srolovitz H, Hamilton E.
    Am J Med Genet; 1985 Aug 01; 21(4):755-60. PubMed ID: 4025400
    [Abstract] [Full Text] [Related]

  • 17. Pancreatic aplasia in a fetus with asplenia-cardiovascular defect-heterotaxy (Ivemark syndrome).
    Konstantinidou A, Sifakis S, Koukoura O, Mantas N, Agrogiannis G, Patsouris E.
    Birth Defects Res A Clin Mol Teratol; 2008 Aug 01; 82(8):601-4. PubMed ID: 18496831
    [Abstract] [Full Text] [Related]

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  • 19. Limb body wall complex: analysis of eight fetuses.
    Cusí V, Torrents M, Vila J, Antich J, Carrera JM.
    Birth Defects Orig Artic Ser; 1996 Aug 01; 30(1):165-70. PubMed ID: 9125325
    [No Abstract] [Full Text] [Related]

  • 20. An 18 week fetus with Elejalde syndrome (acrocephalopolydactylyous dysplasia).
    Nevin NC, Herron B, Armstrong MJ.
    Clin Dysmorphol; 1994 Apr 01; 3(2):180-4. PubMed ID: 8055141
    [Abstract] [Full Text] [Related]

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