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Journal Abstract Search

165 related items for PubMed ID: 1342857

  • 1. Encephalocele, radial defects, cardiac, gastrointestinal, anal, and renal anomalies: a new multiple congenital anomaly (MCA) syndrome?
    Froster-Iskenius U, Meinecke P.
    Clin Dysmorphol; 1992 Jan; 1(1):37-41. PubMed ID: 1342857
    [Abstract] [Full Text] [Related]

  • 2. Encephalocele-radial, cardiac, gastrointestinal, anal/renal anomalies: novel evidence for a new condition?
    Valdez CM, Altmayer SP, Barrow MA, Telles JA, Betat Rda S, Zen PR, Rosa RF.
    Am J Med Genet A; 2014 May; 164A(5):1085-91. PubMed ID: 24648351
    [Abstract] [Full Text] [Related]

  • 3. Genetic syndrome suspicion: examples of clinical approach in the neonatal unit.
    Giuffrè M, De Sanctis L.
    Minerva Pediatr; 2010 Jun; 62(3 Suppl 1):199-201. PubMed ID: 21089741
    [Abstract] [Full Text] [Related]

  • 4. Anorectal anomalies associated with or as part of other anomalies.
    Cuschieri A, EUROCAT Working Group.
    Am J Med Genet; 2002 Jun 15; 110(2):122-30. PubMed ID: 12116249
    [Abstract] [Full Text] [Related]

  • 5. Bronchial anomalies in VACTERL association.
    Kanu A, Tegay D, Scriven R.
    Pediatr Pulmonol; 2008 Sep 15; 43(9):930-2. PubMed ID: 18671276
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  • 7. Lumbocostovertebral syndrome with associated VACTERL anomaly.
    Lyngdoh TS, Mahalik S, Naredi B, Samujh R, Khanna S.
    J Pediatr Surg; 2010 Sep 15; 45(9):e15-7. PubMed ID: 20850610
    [Abstract] [Full Text] [Related]

  • 8. VACTERL with hydrocephalus: a further case with probable autosomal recessive inheritance.
    Corsello G, Giuffrè L.
    Am J Med Genet; 1994 Jan 01; 49(1):137-8. PubMed ID: 8172244
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  • 11. Intrauterine growth retardation, mild frontonasal dysplasia, phocomelic upper limbs with absent thumbs and a variety of internal malformations including choanal atresia, congenital heart defects, polysplenia, absent gall bladder as well as genitourinary anomalies. A possibly "new" MCA syndrome?
    Meinecke P, Peper M.
    Genet Couns; 1992 Jan 01; 3(1):53-6. PubMed ID: 1590982
    [Abstract] [Full Text] [Related]

  • 12. Polysplenia syndrome. A study of five new cases.
    Roguin N, Pelled B, Amikam S, Auslaender L, Riss E.
    Isr J Med Sci; 1978 Sep 01; 14(9):948-53. PubMed ID: 721422
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  • 13. VACTERL association: a new case with biotinidase deficiency and annular pancreas.
    Sezer RG, Aydemir G, Bozaykut A, Paketci C, Aydinoz S.
    Ren Fail; 2012 Sep 01; 34(1):123-5. PubMed ID: 22010814
    [Abstract] [Full Text] [Related]

  • 14. Patterns in multimalformed babies and the question of the relationship between sirenomelia and VACTERL.
    Schüler L, Salzano FM.
    Am J Med Genet; 1994 Jan 01; 49(1):29-35. PubMed ID: 8172248
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  • 15. Polysplenia syndrome and splenic hypoplasia associated with extrahepatic biliary atresia.
    Maksem JA.
    Arch Pathol Lab Med; 1980 Apr 01; 104(4):212-4. PubMed ID: 6892684
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  • 16. Congenital abnormalities associated with limb deficiency defects: a population study based on cases from the Hungarian Congenital Malformation Registry (1975-1984).
    Evans JA, Vitez M, Czeizel A.
    Am J Med Genet; 1994 Jan 01; 49(1):52-66. PubMed ID: 8172251
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  • 17. von Voss-Cherstvoy syndrome: a variable perinatally lethal syndrome of multiple congenital anomalies.
    Lubinsky MS, Kahler SG, Speer IE, Hoyme HE, Kirillova IA, Lurie IW.
    Am J Med Genet; 1994 Sep 01; 52(3):272-8. PubMed ID: 7810558
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  • 18. [Congenital heart disease associated with gastrointestinal malformations].
    Chéhab G, Fakhoury H, Saliba Z, Issa Z, Faour Y, Hammoud D, El-Rassi I.
    J Med Liban; 2007 Sep 01; 55(2):70-4. PubMed ID: 17685118
    [Abstract] [Full Text] [Related]

  • 19. Heterotopic nephrogenic rests in the colon and multiple congenital anomalies: possibly related association.
    Jain D, Martel M, Reyes-Múgica M, Parkash V.
    Pediatr Dev Pathol; 2002 Sep 01; 5(6):587-91. PubMed ID: 12375130
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