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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

136 related items for PubMed ID: 7803123

  • 41. Abnormal myelination in a patient with ring chromosome 18.
    Nakayama J, Hamano K, Shimakura Y, Iwasaki N, Nakahara C, Imoto N, Kobayashi K, Arinami T, Hamaguchi H.
    Neuropediatrics; 1997 Dec; 28(6):335-7. PubMed ID: 9453033
    [Abstract] [Full Text] [Related]

  • 42. Identification of a case of Y:18 translocation using a Y-specific repetitive DNA probe.
    Lau YF, Ying KL, Donnell GN.
    Hum Genet; 1985 Dec; 69(2):102-5. PubMed ID: 2982722
    [Abstract] [Full Text] [Related]

  • 43. [Wooly hair].
    Baliaviĕiene GR.
    Genetika; 1977 Dec; 13(4):739-41. PubMed ID: 892440
    [Abstract] [Full Text] [Related]

  • 44. Subfertile couple with inv(2),inv(9) and 16qh+.
    Srebniak M, Wawrzkiewicz A, Wiczkowski A, Kaźmierczak W, Olejek A.
    J Appl Genet; 2004 Dec; 45(4):477-9. PubMed ID: 15523161
    [Abstract] [Full Text] [Related]

  • 45. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A, Lapunzina P, Palomares M, Molina MA, Galán E, López Pajares I.
    Eur J Med Genet; 2005 Dec; 48(2):159-66. PubMed ID: 16053907
    [Abstract] [Full Text] [Related]

  • 46.
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  • 47. [Perspectives of molecular genetics of hearing disorders].
    Kempf HG, Brändle TU.
    HNO; 1993 Feb; 41(2):68-76. PubMed ID: 8463117
    [Abstract] [Full Text] [Related]

  • 48.
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  • 50. Ring chromosome 21.
    Zergollern L, Muzinić D, Raic Z.
    Acta Med Iugosl; 1989 Feb; 43(2):147-56. PubMed ID: 2741714
    [Abstract] [Full Text] [Related]

  • 51. [Genetic participation in deaf-mutism].
    Bartual R.
    Acta Otorinolaryngol Iber Am; 1969 Feb; 20(3):278-306. PubMed ID: 5816444
    [No Abstract] [Full Text] [Related]

  • 52. A hereditary bisatellite-dicentric supernumerary chromosome in a case of cat-eye syndrome.
    Lüleci G, Bağci G, Kivran M, Lüleci E, Bektaş S, Başaran S.
    Hereditas; 1989 Feb; 111(1):7-10. PubMed ID: 2793513
    [Abstract] [Full Text] [Related]

  • 53. Language and learning skill of hearing-impaired students. Genetic evaluation.
    Smith S, Kimberling WJ.
    ASHA Monogr; 1986 Mar; (23):9-11. PubMed ID: 3730037
    [No Abstract] [Full Text] [Related]

  • 54. Hairy throat: a dominant trait affecting seven members of a family.
    Tsukahara M, Kajii T.
    Clin Dysmorphol; 1992 Jul; 1(3):165-7. PubMed ID: 1342865
    [Abstract] [Full Text] [Related]

  • 55. [Morphologic anomalies of the chromosomes of the 16th pair and the acoustic apparatus].
    Grimaud R, Gilgenkrantz S, Bemol P.
    Acta Otolaryngol; 1967 Jul; 63(2):144-8. PubMed ID: 6032378
    [No Abstract] [Full Text] [Related]

  • 56. Arthritis, bleeding disorder and a chromosome marker--a family study.
    Athreya BH, Bodurtha J, Nichols WW.
    J Rheumatol; 1987 Jun; 14(3):535-9. PubMed ID: 3498037
    [Abstract] [Full Text] [Related]

  • 57. [Phenotype of a ring-chromosome 6 carrier. Clinical and cytogenetic study].
    Cruz-Marin F, Gilgenkrantz S, Gregoire MJ, Beley G, Pierson M.
    J Genet Hum; 1980 Dec; 28(4):95-104. PubMed ID: 7205202
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  • 59. [Karyotype analysis in 44 cases of abnormal chromosome].
    Qiu LL, Lu DS.
    Zhonghua Yi Xue Za Zhi; 1984 Nov; 64(11):691-3. PubMed ID: 6442610
    [No Abstract] [Full Text] [Related]

  • 60. Genetics of deafness: clinical aspects.
    Reardon W.
    Br J Hosp Med; 1984 Nov; 47(7):507-11. PubMed ID: 1581755
    [Abstract] [Full Text] [Related]

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