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Journal Abstract Search

160 related items for PubMed ID: 1114039

  • 1. [Clinical manifestations in 2 cases of trisomy E].
    Białecki M, Słuzewska H.
    Pediatr Pol; 1975 Feb; 50(2):229-33. PubMed ID: 1114039
    [No Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. Trisomy E with multiple congenital anomalies.
    Biswas B, Heycock JB.
    Br J Clin Pract; 1973 Jul; 27(7):269-70. PubMed ID: 4727309
    [No Abstract] [Full Text] [Related]

  • 4. An infant with double trisomy (48,XXX, + 18).
    Jaruratanasirikul S, Jinorose U.
    Am J Med Genet; 1994 Jan 15; 49(2):207-10. PubMed ID: 8116670
    [Abstract] [Full Text] [Related]

  • 5. Trisomy 18 (Edwards syndrome) in Delaware.
    Morallo LM, Rosenblum H, Esterly KL, Johnson WD, Storlazzi JJ, Narvaez AC, Borgaonkar DS.
    Del Med J; 1983 Jan 15; 55(1):27-30. PubMed ID: 6840358
    [No Abstract] [Full Text] [Related]

  • 6. Trisomy 18: Edward's syndrome (a case report of 3 cases).
    Bharucha BA, Agarwal UM, Savliwala AS, Kolluri R, Kumta NB.
    J Postgrad Med; 1983 Apr 15; 29(2):129-32. PubMed ID: 6631764
    [No Abstract] [Full Text] [Related]

  • 7. [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 15; 24(2):60-73. PubMed ID: 5399531
    [No Abstract] [Full Text] [Related]

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  • 9. Unusual extra chromosomes in the mother of a 18-trisomy newborn.
    Mori M, Sasaki M, Makino S, Fujimoto S.
    Jinrui Idengaku Zasshi; 1969 Sep 15; 14(2):145-50. PubMed ID: 5392345
    [No Abstract] [Full Text] [Related]

  • 10. [12 p trisomy. A new case (author's transl)].
    Kubryk N, Prieur M, Borde M.
    Ann Pediatr (Paris); 1980 Dec 15; 27(10):695-9. PubMed ID: 7212558
    [No Abstract] [Full Text] [Related]

  • 11. Partial trisomy 9q-in a polymalformed new-born infant. Karyotype: 47,XX, + del (9) (q33).
    Fryns JP, Smeets E, Eggermont E, Delire C, Van den Berghe H.
    Acta Paediatr Belg; 1978 Dec 15; 31(4):237-40. PubMed ID: 742362
    [No Abstract] [Full Text] [Related]

  • 12. ["De novo" partial trisomy 16p (author's transl)].
    Gabarrón Llamas J, Cabrerizo Portero D, Montserrat Bernal F, Rodríguez Costa T, Cabrerizo Merino C, Rodríguez López F.
    An Esp Pediatr; 1981 Dec 15; 15(6):587-91. PubMed ID: 7337311
    [Abstract] [Full Text] [Related]

  • 13. [9p trisomy syndrome. Two new cases (author's transl)].
    Martín Sánchez A, Delicado A, Izquierdo M, Oliver A, López Pajares I, Gracia R, Peralta A.
    An Esp Pediatr; 1981 May 15; 14(5):344-51. PubMed ID: 7294523
    [Abstract] [Full Text] [Related]

  • 14. [Morphologic abnormality due to duplication of chromosome 17 (46,XY,17q+) in a newborn infant].
    Fouquette B, Rosenfeld R, Cadotte M.
    Union Med Can; 1974 Aug 15; 103(8):1404-8. PubMed ID: 4849205
    [No Abstract] [Full Text] [Related]

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  • 16. Partial trisomy for different segments of chromosome 13 in several individuals of the same family.
    Wilroy RS, Summitt RL, Martens PR.
    Birth Defects Orig Artic Ser; 1975 Aug 15; 11(5):217-22. PubMed ID: 1218217
    [No Abstract] [Full Text] [Related]

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  • 19. [Children with chromosome abnormalities in a pediatric department].
    Nielsen J, Friedrich U, Holm V, Sveinsson S.
    Ugeskr Laeger; 1973 Feb 19; 135(8):408-15. PubMed ID: 4265917
    [No Abstract] [Full Text] [Related]

  • 20. Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9.
    Shapiro SD, Hansen KL, Littlefield CA.
    Am J Med Genet; 1985 Feb 19; 20(2):271-6. PubMed ID: 3976720
    [Abstract] [Full Text] [Related]

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