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Journal Abstract Search

92 related items for PubMed ID: 5310105

  • 1. [A case of 47XY, (?18q-)+].
    Lejeune J, Berger R, Rethoré MO, Attal C.
    Ann Genet; 1970 Mar; 13(1):47-51. PubMed ID: 5310105
    [No Abstract] [Full Text] [Related]

  • 2. Trisomy of chromosome 16 in a neonate, 47XY,?16+.
    Taylor AI.
    J Med Genet; 1971 Mar; 8(1):123-5. PubMed ID: 5098068
    [No Abstract] [Full Text] [Related]

  • 3. A case of 18q- in a t(18q-;6p+) family.
    Jacobsen P, Mikkelsen M, Niebuhr E, de Grouchy J.
    Ann Genet; 1971 Mar; 14(1):41-8. PubMed ID: 5314293
    [No Abstract] [Full Text] [Related]

  • 4. [Rare case of mosaicism for chromosome 18, karyotype: 46, XX, del(18) (p11)/46, XX, i(18q)].
    Badalian LO, Mutovin GR, Malygina NA, Petrukhin AS.
    Genetika; 1983 Nov; 19(11):1912-5. PubMed ID: 6686175
    [Abstract] [Full Text] [Related]

  • 5. [A case of 18q-syndrome].
    Lejeune J, Berger R, Rethoré MO, Vialatte J.
    J Genet Hum; 1969 Oct; 17(3):423-8. PubMed ID: 5387418
    [No Abstract] [Full Text] [Related]

  • 6. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation].
    Fioretti G, Pagano L, Renda S, Festa B, Rinaldi A, Celona A, Casullo C, Stabile M, Cavaliere ML, Ventruto V.
    Minerva Pediatr; 1980 Jun 30; 32(12):807-14. PubMed ID: 7464734
    [No Abstract] [Full Text] [Related]

  • 7. An unbalanced karyotype in a translocation (Cq-,Aq+) pedigree.
    Smith GF, Shear CS, Jalowayski I, Akesson HO.
    J Ment Defic Res; 1969 Jun 30; 13(2):123-9. PubMed ID: 5794286
    [No Abstract] [Full Text] [Related]

  • 8. The syndrome associated with the partial deletion of the long arms of chromosome 18 (18q-).
    Parker CE, Mavalwala J, Koch R, Hatashita A, Derencsenyi A.
    Calif Med; 1972 Oct 30; 117(4):65-71. PubMed ID: 5075725
    [No Abstract] [Full Text] [Related]

  • 9. Aneusomie de recombinaison: rearrangement between paternal chromosomes 4 and 18 yielding offspring with features of the 18q- syndrome.
    Hoehn H, Sander C, Sander LZ.
    Ann Genet; 1971 Sep 30; 14(3):187-92. PubMed ID: 5315465
    [No Abstract] [Full Text] [Related]

  • 10. [D trisomy. 2 cases with characteristic phenotype].
    Giovannucci ML, Calabri G, Paoli A.
    Riv Clin Pediatr; 1969 Sep 30; 82():320-9. PubMed ID: 5405486
    [No Abstract] [Full Text] [Related]

  • 11. [Small supernumerary metacentric chromosome in a sister of a child with trisomy 21].
    Walbaum R.
    Ann Pediatr (Paris); 1971 Sep 30; 18(6):455-63. PubMed ID: 5564916
    [No Abstract] [Full Text] [Related]

  • 12. Double trisomy 48,XXX,+ 18 in a newborn.
    Rosenfeld W, Verma RS, Jhaveri RC, Salazar D, Dosik H.
    Am J Med Genet; 1981 Sep 30; 8(1):67-71. PubMed ID: 7246607
    [Abstract] [Full Text] [Related]

  • 13. [Cp trisomy: a new syndrome].
    Canu JM, Buentello L, Armendares S.
    Ann Genet; 1971 Sep 30; 14(3):177-86. PubMed ID: 5315464
    [No Abstract] [Full Text] [Related]

  • 14. [A case of double trisomy: 48,XXX,18+].
    Emberger JM, Sarran R, Balzing P.
    Ann Genet; 1971 Dec 30; 14(4):301-3. PubMed ID: 5316134
    [No Abstract] [Full Text] [Related]

  • 15. [Contribution and considerations on cranio-facial abnormalities caused by chromosomic aberrations in children].
    Infortuna M, Gattarello A, Corrado F.
    Pediatr Med Chir; 1984 Dec 30; 6(3):415-23. PubMed ID: 6533589
    [Abstract] [Full Text] [Related]

  • 16. Partial trisomy of chromosome 18 (pter leads to q11): a discussion on the identification of the critical segment.
    San Martin V, Fernandez-Novoa C, Hevia A, Novales A, Fornell J, Galera H.
    Ann Genet; 1981 Dec 30; 24(4):248-50. PubMed ID: 6977308
    [Abstract] [Full Text] [Related]

  • 17. Structural abnormalities of chromosome 18. I. A case of 18q-, with autopsy findings.
    Fraccaro M, Hulten M, Ivemark BI, Lindsten J, Tiepolo L, Zetterqvist P.
    Ann Genet; 1971 Dec 30; 14(4):275-80. PubMed ID: 5316132
    [No Abstract] [Full Text] [Related]

  • 18. [Familial observation of partial trisomy 6, and probable partial monosomy 18q by parental translocation].
    D'Emma C, Crippa L, Delozier C, Michail E, Graber P.
    J Genet Hum; 1982 Mar 30; 30(1):39-50. PubMed ID: 7130955
    [Abstract] [Full Text] [Related]

  • 19. [A recent case of partial deletion of short arm of chromosome 18].
    Vaillaud JC, Martin J, Ayraud N.
    Ann Genet; 1970 Jun 30; 13(2):120-2. PubMed ID: 5310694
    [No Abstract] [Full Text] [Related]

  • 20. [The problem of trisomy 22].
    Walbaum R, Samaille G, Scharfman W, Maillard E.
    Pediatrie; 1970 Mar 30; 25(2):133-43. PubMed ID: 5443264
    [No Abstract] [Full Text] [Related]

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