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Journal Abstract Search

290 related items for PubMed ID: 5306714

  • 21. Results of 538 chromosome studies on patients referred for cytogenetic analysis.
    Mulcahy MT, Jenkyn J.
    Med J Aust; 1972 Dec 09; 2(24):1333-8. PubMed ID: 4265391
    [No Abstract] [Full Text] [Related]

  • 22. Unusual extra chromosomes in the mother of a 18-trisomy newborn.
    Mori M, Sasaki M, Makino S, Fujimoto S.
    Jinrui Idengaku Zasshi; 1969 Sep 09; 14(2):145-50. PubMed ID: 5392345
    [No Abstract] [Full Text] [Related]

  • 23. [Ocular manifestations of trisomy 18].
    Ardouin M, Urvoy M, Lautridou A, Le Marec B, Senecal J.
    Arch Ophtalmol Rev Gen Ophtalmol; 1972 Sep 09; 32(6):457-76. PubMed ID: 4264548
    [No Abstract] [Full Text] [Related]

  • 24. Developmental and other pathologic changes in syndromes caused by chromosome abnormalities.
    Gilbert EF, Opitz JM.
    Perspect Pediatr Pathol; 1982 Sep 09; 7():1-63. PubMed ID: 6214761
    [No Abstract] [Full Text] [Related]

  • 25. [On three cases of C trisomy].
    Lejeune J, Dutrillaux B, Rethoré MO, Berger R, Debray H, Veron P, Gorce F, Grossiord A.
    Ann Genet; 1969 Mar 09; 12(1):28-35. PubMed ID: 5306709
    [No Abstract] [Full Text] [Related]

  • 26. [Clinical manifestations in 2 cases of trisomy E].
    Białecki M, Słuzewska H.
    Pediatr Pol; 1975 Feb 09; 50(2):229-33. PubMed ID: 1114039
    [No Abstract] [Full Text] [Related]

  • 27. 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 09; 55(1):27-30. PubMed ID: 6840358
    [No Abstract] [Full Text] [Related]

  • 28. Double trisomy (48,XXX, +18).
    Tsukahara M, Fukuda M, Furukawa S, Kondoh O.
    Am J Med Genet; 1994 Aug 15; 52(2):244. PubMed ID: 7802021
    [No Abstract] [Full Text] [Related]

  • 29. [Chromosome 18 long arm deletion. A case with unusual dermatoglyphics].
    Le Marec B, Lessard M, Renault A, Coutel Y.
    Pediatrie; 1971 Aug 15; 26(7):749-57. PubMed ID: 5118994
    [No Abstract] [Full Text] [Related]

  • 30. 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]

  • 31. Partial trisomy 16q in the son resulting from paternal 16/21 translocation.
    Kosanović M, Lopicić L, Diklić V, Nikolis J.
    Acta Med Iugosl; 1983 Apr 15; 37(4):335-40. PubMed ID: 6650222
    [No Abstract] [Full Text] [Related]

  • 32. An unbalanced karyotype in a translocation (Cq-,Aq+) pedigree.
    Smith GF, Shear CS, Jalowayski I, Akesson HO.
    J Ment Defic Res; 1969 Jun 15; 13(2):123-9. PubMed ID: 5794286
    [No Abstract] [Full Text] [Related]

  • 33. A case of nondisjunction of chromosome 21 (47,X,Yqs,+21) in an Indian family with Yqs.
    Reddy KS, Thomas IM, Narayanan HS.
    Ann Genet; 1984 Jun 15; 27(3):194-6. PubMed ID: 6334487
    [Abstract] [Full Text] [Related]

  • 34. Human chromosome analysis: methodology and applications.
    Larson L.
    Am J Med Technol; 1983 Oct 15; 49(10):687-98. PubMed ID: 6228140
    [Abstract] [Full Text] [Related]

  • 35. [Trisomy 10p as a result of familial 10/22 translocation].
    Zergollern L, Begovic D, Muzinić D.
    Acta Med Iugosl; 1980 Oct 15; 34(2):113-22. PubMed ID: 7405617
    [No Abstract] [Full Text] [Related]

  • 36. [Dermatoglyphics and congenital malformation (author's transl)].
    Shiono K.
    Hokkaido Igaku Zasshi; 1978 Nov 15; 52(6):237-46. PubMed ID: 147230
    [No Abstract] [Full Text] [Related]

  • 37. Phenotypic overlapping of autosomal trisomy syndromes and its significance.
    Balakrishnan S, Puri RK, Bhargava I.
    Indian Pediatr; 1971 Jul 15; 8(7):336-41. PubMed ID: 5113591
    [No Abstract] [Full Text] [Related]

  • 38. [Diagnosis and prevention of chromosome aberrations].
    Sachs ES, van Hemel JO.
    Ned Tijdschr Geneeskd; 1982 Dec 04; 126(49):2236-44. PubMed ID: 6217426
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. 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 04; 24(4):248-50. PubMed ID: 6977308
    [Abstract] [Full Text] [Related]

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