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Journal Abstract Search

496 related items for PubMed ID: 5315464

  • 1. [Cp trisomy: a new syndrome].
    Canu JM, Buentello L, Armendares S.
    Ann Genet; 1971 Sep; 14(3):177-86. PubMed ID: 5315464
    [No Abstract] [Full Text] [Related]

  • 2. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
    Tal'vik TA, Mikel'saar AV, Mikel'saar RV.
    Sov Genet; 1974 Jun 01; 8(5):651-7. PubMed ID: 4413436
    [No Abstract] [Full Text] [Related]

  • 3. [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].
    Rethoré MO, Larget-Piet L, Abonyi D, Boeswillwald M, Berger R, Carpentier S, Cruveiller J, Dutrillau B, Lafourcade J, Penneau M, Lejeune J.
    Ann Genet; 1970 Dec 01; 13(4):217-32. PubMed ID: 5313386
    [No Abstract] [Full Text] [Related]

  • 4. [Partial 7q trisomy].
    Serville F, Broustet A, Sandler B, Bourdeau MJ, Leloup M.
    Ann Genet; 1975 Mar 01; 18(1):67-70. PubMed ID: 1080040
    [Abstract] [Full Text] [Related]

  • 5. [Trisomy of group C (47, XX, C+)].
    Emberger JM, Rey J, Rieu D, Dossa D, Bonnet H, Jean R.
    Arch Fr Pediatr; 1970 Mar 01; 27(10):1081-8. PubMed ID: 5495708
    [No Abstract] [Full Text] [Related]

  • 6. Partial trisomy 9 in the case of familial translocation 8/9 mat.
    Schwanitz G, Schamberger U, Rott HD, Wieczorek V.
    Ann Genet; 1974 Sep 01; 17(3):163-6. PubMed ID: 4548816
    [No Abstract] [Full Text] [Related]

  • 7. [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
    [Abstract] [Full Text] [Related]

  • 8. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].
    Giovannelli G, Forabosco A, Dutrillaux B.
    Ann Genet; 1974 Jun 01; 17(2):119-24. PubMed ID: 4547939
    [No Abstract] [Full Text] [Related]

  • 9. [Partial trisomy 11q;22q (author's transl)].
    Benítez J, Ayuso C, García Aparicio J, Sáez E, Pérez Sotelo A, Bello MJ.
    An Esp Pediatr; 1981 Sep 01; 15(3):293-300. PubMed ID: 7332142
    [No Abstract] [Full Text] [Related]

  • 10. Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.
    García-Cruz D, García-Esquivel L, Rivera H, Vaca G, Rolón A, Cantú JM.
    Ann Genet; 1985 Sep 01; 28(3):193-6. PubMed ID: 3879157
    [Abstract] [Full Text] [Related]

  • 11. Partial trisomy of chromosome 11: a case report.
    Falk RE, Carrel RE, Valente M, Crandall BF, Sparkes RS.
    Am J Ment Defic; 1973 Jan 01; 77(4):383-8. PubMed ID: 4706396
    [No Abstract] [Full Text] [Related]

  • 12. The 12p trisomy syndrome.
    Armendares S, Salamanca F, Nava S, Ramirez S, Cantu JM.
    Ann Genet; 1975 Jun 01; 18(2):89-94. PubMed ID: 1081370
    [Abstract] [Full Text] [Related]

  • 13. Partial trisomy 10q occurring in a family with a reciprocal translocation t(10;18)(q25;q23).
    Kroyer S, Niebuhr E.
    Ann Genet; 1975 Mar 01; 18(1):50-5. PubMed ID: 50043
    [Abstract] [Full Text] [Related]

  • 14. [Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case].
    Ayraud N, Galiana A, Llyod M, Deswarte M.
    Ann Genet; 1976 Mar 01; 19(1):65-8. PubMed ID: 1084126
    [Abstract] [Full Text] [Related]

  • 15. [Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11)].
    Rethoré MO, Kaplan JC, Junien C, Cruveiller J, Dutrillaux B, Aurias A, Carpentier S, Lafourcade J, Lejeune.
    Ann Genet; 1975 Jun 01; 18(2):81-7. PubMed ID: 1081369
    [Abstract] [Full Text] [Related]

  • 16. [Interstitial deletion of the long arm of one 11 chromosome].
    Taillemite JL, Morlier BG, Roux C.
    Ann Genet; 1975 Mar 01; 18(1):61-3. PubMed ID: 1080039
    [Abstract] [Full Text] [Related]

  • 17. Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8.
    Pai GS, Thomas GH, Leonard CO, Ward JC, Valle DL, Pyeritz RE.
    Johns Hopkins Med J; 1979 Oct 01; 145(4):162-9. PubMed ID: 491337
    [No Abstract] [Full Text] [Related]

  • 18. A new syndrome of proximal deletion of the long arm of chromosome 1: 1q21-23 leads to 1q25.
    Taysi K, Sekhon GS, Hillman RE.
    Am J Med Genet; 1982 Dec 01; 13(4):423-30. PubMed ID: 7158642
    [No Abstract] [Full Text] [Related]

  • 19. [A case of translocation t(Cp-; Bp+)].
    Ricci N, Ventimiglia B, Dallapiccola B, Preto G.
    Ann Genet; 1967 Jun 01; 10(2):82-5. PubMed ID: 5298977
    [No Abstract] [Full Text] [Related]

  • 20. A partial trisomy 5p syndrome.
    Opitz JM, Patau K.
    Birth Defects Orig Artic Ser; 1975 Jun 01; 11(5):191-200. PubMed ID: 1218213
    [No Abstract] [Full Text] [Related]

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