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Journal Abstract Search

240 related items for PubMed ID: 1391972

  • 1. Terminal deletion of the short arm of chromosome 3.
    Asai M, Ito Y, Iguchi T, Ito J, Okada N, Oishi H.
    Jpn J Hum Genet; 1992 Jun; 37(2):163-8. PubMed ID: 1391972
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  • 2. De novo interstitial deletion of the long arm of chromosome 7:46,XY,del(7)(q23;q32).
    Martin-Pont B, Pilczer C, Dandine M, Tamboise A.
    Ann Genet; 1985 Jun; 28(4):251-3. PubMed ID: 3879441
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  • 3. Terminal deletion of the long arm of chromosome 4. Report of a case of 46, XY, del(4)(q31) and review of 4q- syndrome.
    Yu CW, Chen H, Baucum RW, Hand AM.
    Ann Genet; 1981 Jun; 24(3):158-61. PubMed ID: 6974525
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  • 4. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3).
    Copelli S, del Rey G, Heinrich J, Coco R.
    Am J Med Genet; 1995 Jan 02; 55(1):77-9. PubMed ID: 7702102
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  • 5. Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.
    Zenger-Hain JL, Roberson J, Van Dyke DL, Weiss L.
    Am J Med Genet; 1993 Jun 01; 46(4):438-40. PubMed ID: 7689299
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  • 6. Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3.
    Narahara K, Kikkawa K, Murakami M, Hiramoto K, Namba H, Tsuji K, Yokoyama Y, Kimoto H.
    Am J Med Genet; 1990 Feb 01; 35(2):269-73. PubMed ID: 2178418
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  • 7. [Terminal partial mosaic monosomy of the short arm of chromosome 3, in discordant monozygotic twins, 46,XY/46,XY, del (3) (p25)].
    Bueno I, Olivares JL, Olmedillas MJ, Abad M, Bueno M.
    An Esp Pediatr; 1987 Mar 01; 26(3):187-90. PubMed ID: 3579058
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  • 10. Interstitial deletion of the short arm of chromosome 1 (46XY, del(1)(p13p22.3)).
    Mattia FR, Wardinsky TD, Tuttle DJ, Grix A, Smith KA, Walling P.
    Am J Med Genet; 1992 Nov 15; 44(5):551-4. PubMed ID: 1481806
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  • 12. A case of interstitial 1q deletion [46,XY,del(q25q32.1)].
    Hamano S, Fukushima Y, Yamada T, Shimizu H, Okuyama M, Ito F, Maekawa K.
    Ann Genet; 1987 Nov 15; 30(2):105-8. PubMed ID: 3314663
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  • 13. 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
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  • 14. Terminal deletion of the short arm of chromosome 3, del(3pter-p25): a recognizable syndrome.
    Schwyzer U, Binkert F, Caflisch U, Baumgartner B, Schinzel A.
    Helv Paediatr Acta; 1987 Jul 01; 42(4):309-15. PubMed ID: 3443553
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  • 15. Chromosome 10qter deletion syndrome: a review and report of three new cases.
    Wulfsberg EA, Weaver RP, Cunniff CM, Jones MC, Jones KL.
    Am J Med Genet; 1989 Mar 01; 32(3):364-7. PubMed ID: 2658586
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  • 17. Interstitial deletion 13q: further delineation of the syndrome by clinical and high-resolution chromosome analysis of five patients.
    Tranebjaerg L, Nielsen KB, Tommerup N, Warburg M, Mikkelsen M.
    Am J Med Genet; 1988 Apr 01; 29(4):739-53. PubMed ID: 3400720
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  • 19. Terminal deletion of 6p: report of a new case.
    Plaja A, Vidal R, Soriano D, Bou X, Vendrell T, Mediano C, Pueyo JM, Labraña X, Sarret E.
    Ann Genet; 1994 Apr 01; 37(4):196-9. PubMed ID: 7710255
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  • 20. Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature.
    Taysi K, Strauss AW, Yang V, Padmalatha C, Marshall RE.
    Ann Genet; 1982 Apr 01; 25(3):141-4. PubMed ID: 6982660
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