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Journal Abstract Search

137 related items for PubMed ID: 5034791

  • 81. Spectrum of clinical and autopsy findings in trisomy 18 syndrome.
    Moerman P, Fryns JP, Goddeeris P, Lauweryns JM.
    J Genet Hum; 1982 Mar; 30(1):17-38. PubMed ID: 7130954
    [Abstract] [Full Text] [Related]

  • 82. [Trisomy 18 in 2 newborn infants with rare abnormalities in one of them].
    Bruni L, Castello MA, Crucioli V, Zucco V.
    Riv Ostet Ginecol; 1969 Feb; 24(2):60-73. PubMed ID: 5399531
    [No Abstract] [Full Text] [Related]

  • 83. [Apropos of trisomy 18 - a study of 4 observations].
    Gilgenkrantz S, Sapelier J, Thiriet M, Kahn C, Pierson M.
    Ann Genet; 1967 Mar; 10(1):32-8. PubMed ID: 5300124
    [No Abstract] [Full Text] [Related]

  • 84.
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  • 85. [Edwards syndrome in a pair of twins].
    Lapi E, Benedetti A, Biondi A.
    Minerva Ginecol; 1981 Dec; 33(12):1151-4. PubMed ID: 7335241
    [No Abstract] [Full Text] [Related]

  • 86. Rapid karyotypic diagnosis of a case of trisomy 18 in the neonatal intensive care unit.
    Arbisser A, Moore CM, Adcock EW, Morriss FH.
    South Med J; 1977 Mar; 70(3):366-7. PubMed ID: 847492
    [Abstract] [Full Text] [Related]

  • 87. FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotype.
    Chu TW, Teebi AS, Gibson L, Breg WR, Yang-Feng TL.
    Am J Med Genet; 1994 Aug 01; 52(1):92-6. PubMed ID: 7977471
    [Abstract] [Full Text] [Related]

  • 88. [Partial trisomy of the proximal part of the long arm of chromosome 13].
    Saura R, Longy M, Serville F, Sautarel M, Renouil M, Sandler B.
    Pediatrie; 1982 Sep 01; 37(6):473-7. PubMed ID: 7155728
    [No Abstract] [Full Text] [Related]

  • 89.
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  • 90. Trisomy 18 with multiple rare malformations: report of one case.
    Su PH, Chen JY, Hsu CH, Chen SJ, Chan SW, Lin LL.
    Acta Paediatr Taiwan; 2007 Sep 01; 48(5):272-5. PubMed ID: 18254577
    [Abstract] [Full Text] [Related]

  • 91. Cytogenetic and molecular analysis of trisomy 9. Case report and review.
    Zelante L, Notarangelo A, Croce AI, Piemontese MR, Gasparini P.
    Ann Genet; 1994 Sep 01; 37(1):21-5. PubMed ID: 8010708
    [Abstract] [Full Text] [Related]

  • 92. [Phenotype of trisomy 9].
    Pfeiffer RA, Müller R.
    Monatsschr Kinderheilkd; 1984 Oct 01; 132(10):797-800. PubMed ID: 6513939
    [Abstract] [Full Text] [Related]

  • 93.
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  • 94.
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  • 95. Anatomic studies in the 18-trisomy syndrome.
    Barash BA, Freedman L, Opitz JM.
    Birth Defects Orig Artic Ser; 1970 Oct 01; 6(4):3-15. PubMed ID: 5524827
    [No Abstract] [Full Text] [Related]

  • 96. A case of multiple congenital anomalies--D1 trisomy syndrome.
    Jayasuriya D, Mirando EH.
    Ceylon Med J; 1969 Sep 01; 14(3):139-40. PubMed ID: 5370224
    [No Abstract] [Full Text] [Related]

  • 97. [Edward's syndrome: trisomy 18].
    Behrens R, Greiner P, Böhm N.
    Med Welt; 1980 Mar 14; 31(11):400-3. PubMed ID: 7392917
    [No Abstract] [Full Text] [Related]

  • 98. Genetics of atrial septal defect.
    Sánchez Cascos A.
    Arch Dis Child; 1972 Aug 14; 47(254):581-8. PubMed ID: 4261647
    [Abstract] [Full Text] [Related]

  • 99. [Multiple congenital anomalies in a 10-year-old girl with trisomy and mosaicism of the chromosomes in group E].
    Gebala A, Dobrzańska A, Warakomska-Grzycka S, Mach W.
    Pol Tyg Lek; 1969 May 12; 24(19):716-9. PubMed ID: 5804311
    [No Abstract] [Full Text] [Related]

  • 100. A case of Edward's syndrome with pseudodicentric isochromosome 18: 46,XY,i dic(18) (p11::p11).
    Fioretti G, Stabile M, Pagano L, Rinaldi A, Rolando D, Trapassi C, de Tollis G, Ventruto V.
    Ann Genet; 1982 May 12; 25(2):116-8. PubMed ID: 6984627
    [No Abstract] [Full Text] [Related]

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