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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

321 related items for PubMed ID: 2241091

  • 1. Interstitial deletion of the band 4p15.3 defined by sequential replication banding.
    Davies J, Voullaire L, Bankier A.
    Ann Genet; 1990; 33(2):92-5. PubMed ID: 2241091
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  • 3. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
    Piovani G, Borsani G, Bertini V, Kalscheuer VM, Viertel P, Bellotti D, Valseriati D, Barlati S.
    Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
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  • 5. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).
    Gorski JL, Cox BA, Kyine M, Uhlmann W, Glover TW.
    Am J Med Genet; 1989 Mar; 32(3):350-2. PubMed ID: 2729355
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  • 6. Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndrome.
    Fryns JP, Yang-Aisheng, Kleczkowska A, Lemmens F, Vandecasseye W, van den Berghe H.
    Ann Genet; 1989 Mar; 32(1):59-61. PubMed ID: 2751251
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  • 8. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
    Mdzin R, Ko C, Abdul Latif Z, Zakaria Z.
    Singapore Med J; 2008 Nov; 49(11):e336-9. PubMed ID: 19037546
    [Abstract] [Full Text] [Related]

  • 9. A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4.
    Beall MH, Falk RE, Ying KL.
    Am J Med Genet; 1988 Nov; 31(3):553-7. PubMed ID: 3067576
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  • 10. Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.
    Chitayat D, Ruvalcaba RH, Babul R, Teshima IE, Posnick JC, Vekemans MJ, Scarpelli H, Thuline H.
    Am J Med Genet; 1995 Jan 16; 55(2):147-54. PubMed ID: 7717413
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  • 11. Thrombocytopenia and cleft hand in monosomy 21.
    Vogels A, de Smet L, van den Berghe H, Fryns JP.
    Genet Couns; 1994 Jan 16; 5(1):67-71. PubMed ID: 8031538
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  • 12. Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3.
    Meng J, Fujita H, Nagahara N, Kashiwai A, Yoshioka Y, Funato M.
    Am J Med Genet; 1992 Jul 01; 43(4):747-50. PubMed ID: 1621768
    [Abstract] [Full Text] [Related]

  • 13. Normal phenotype and slight mental retardation in de novo distal 8p deletion (8pter----8p23.1:).
    Fryns JP, Kleczkowska A, Vogels A, Van den Berghe H.
    Ann Genet; 1989 Jul 01; 32(3):171-3. PubMed ID: 2573313
    [Abstract] [Full Text] [Related]

  • 14. 7p deletion syndrome: an adult with mild manifestations.
    Grebe TA, Stevens MA, Byrne-Essif K, Cassidy SB.
    Am J Med Genet; 1992 Sep 01; 44(1):18-23. PubMed ID: 1519644
    [Abstract] [Full Text] [Related]

  • 15. De novo partial monosomy 21 with unusual karyotype.
    Al-Awadi SA, Naguib KK, Teebi AS, Sundareshan TS.
    Jinrui Idengaku Zasshi; 1986 Mar 01; 31(1):45-8. PubMed ID: 3735757
    [No Abstract] [Full Text] [Related]

  • 16. A child with multiple congenital anomalies and karyotype 46,XY,del(14)(q31q32.3): further delineation of chromosome 14 interstitial deletion syndrome.
    Gorski JL, Uhlmann WR, Glover TW.
    Am J Med Genet; 1990 Dec 01; 37(4):471-4. PubMed ID: 2260590
    [Abstract] [Full Text] [Related]

  • 17. Langer-Giedion syndrome with interstitial 8q-deletion.
    Zabel BU, Baumann WA.
    Am J Med Genet; 1982 Mar 01; 11(3):353-8. PubMed ID: 7081298
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  • 18. Gardner syndrome in a boy with interstitial deletion of the long arm of chromosome 5.
    Kobayashi T, Narahara K, Yokoyama Y, Ueyama S, Mohri O, Fujii T, Fujimoto M, Ohtsuki S, Tsuji K, Seino Y.
    Am J Med Genet; 1991 Dec 15; 41(4):460-3. PubMed ID: 1776638
    [Abstract] [Full Text] [Related]

  • 19. Loss of the N-myc oncogene in a patient with a small interstitial deletion of the short arm of chromosome 2.
    Saal HM, King LJ, Zimmerman D, Johnson RC, Carr AG, Samango-Sprouse CA, Stanley W.
    Am J Med Genet; 1996 Dec 30; 66(4):373-7. PubMed ID: 8989454
    [Abstract] [Full Text] [Related]

  • 20. Interstitial deletion of chromosome 2 (p23p25).
    Penchaszadeh VB, Dowling PK, Davis JG, Schmidt R, Wapnir RA.
    Am J Med Genet; 1987 Jul 30; 27(3):701-6. PubMed ID: 3477099
    [Abstract] [Full Text] [Related]

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