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Journal Abstract Search

183 related items for PubMed ID: 953215

  • 1. Trisomy C and cystic dysplasia of kidneys, liver and pancreas.
    Blair JD.
    Birth Defects Orig Artic Ser; 1976; 12(5):139-49. PubMed ID: 953215
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  • 2. Renal-hepatic-pancreatic dysplasia: a syndrome reconsidered.
    Bernstein J, Chandra M, Creswell J, Kahn E, Malouf NN, McVicar M, Weinberg AG, Wybel RE.
    Am J Med Genet; 1987 Feb; 26(2):391-403. PubMed ID: 3812591
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  • 3. Renal-hepatic-pancreatic dysplasia and its variants.
    Lurie IW, Kirillova IA, Novikova IV, Burakovski IV.
    Genet Couns; 1991 Feb; 2(1):17-20. PubMed ID: 1741971
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  • 6. The Meckel syndrome: clinicopathological findings in 67 patients.
    Salonen R.
    Am J Med Genet; 1984 Aug; 18(4):671-89. PubMed ID: 6486167
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  • 7. Ontogeny of renal dysplasia in Ivemark syndrome: light and immunohistochemical characterization.
    Abbi R, Daum F, Kahn E.
    Ann Clin Lab Sci; 1999 Aug; 29(1):9-17. PubMed ID: 10074963
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  • 8. [Renal polycystosis in the newborn. Clinico-pathological observations. Mosaic trisomy C].
    Beaudoing A, Bost M, Rambaud P, Pasquier B, Dumontel C.
    Cesk Pediatr; 1972 May; 27(5):223-4. PubMed ID: 5030319
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  • 9. Renal, pancreatic and hepatic dysplasia sequence.
    Carles D, Serville F, Dubecq JP, Gonnet JM.
    Eur J Pediatr; 1988 May; 147(4):431-2. PubMed ID: 3396599
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  • 10. [Trisomy 10q24--10qter].
    Dutrillaux B, Laurent C, Bernasconi S, Lejeune J.
    Ann Genet; 1975 Dec; 18(4):217-22. PubMed ID: 1083188
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  • 11. Trisomy 10p, due to an unusual translocation.
    Orye E, Van Haesebrouck P, Van Coster R, Van Mele B.
    J Genet Hum; 1985 Jan; 33(1):63-6. PubMed ID: 3981144
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  • 12. Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18?
    Shashi V, Golden WL, von Kap-Herr C, Wilson WG.
    Am J Med Genet; 1996 Mar 01; 62(1):38-41. PubMed ID: 8779322
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  • 14. [Partial trisomy 14q II.--Partial trisomy 14q due to a maternal t(12; 14) (q24.4; q21)].
    Turleau C, Grouchy J, Bocquentin F, Roubin M, Colin FC.
    Ann Genet; 1975 Mar 01; 18(1):41-4. PubMed ID: 1080037
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  • 15. The pathology of trisomy 13 syndrome. A study of 12 cases.
    Moerman P, Fryns JP, van der Steen K, Kleczkowska A, Lauweryns J.
    Hum Genet; 1988 Dec 01; 80(4):349-56. PubMed ID: 3198112
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  • 19. Oligohydramnios syndrome and XYY karyotype.
    Côté GB, Tsomi K, Papadakou-Lagoyanni S, Petmezaki S.
    Ann Genet; 1978 Dec 01; 21(4):226-8. PubMed ID: 314260
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  • 20. [Apropos of a case of trisomy D (15)].
    Ferrero AM, Marca L, Satolli E, Console V, Airaghi M, Valagussa E.
    Minerva Pediatr; 1973 Mar 10; 25(8):338-42. PubMed ID: 4197713
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