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Journal Abstract Search

109 related items for PubMed ID: 3499842

  • 1. Moderate mental retardation and mild dysmorphic syndrome in proximal 7q interstitial deletion.
    Fryns JP, Kleczkowska A, Van den Berghe H.
    Ann Genet; 1987; 30(2):111-2. PubMed ID: 3499842
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  • 2. Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infant.
    Gillar PJ, Kaye CI, Ryan SG, Moore CM.
    Am J Med Genet; 1992 Sep 15; 44(2):138-41. PubMed ID: 1456281
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  • 3. Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases.
    Poissonnier M, Turleau C, Olivier-Martin M, Milleret-Proyart MJ, Prieur M, Dubos M, Cabanis MO, Mugneret F, Blanc P, Noel L.
    Ann Genet; 1992 Sep 15; 35(3):146-51. PubMed ID: 1466563
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  • 4. Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation.
    Ahlbom BE, Sidenvall R, Annerén G.
    Am J Med Genet; 1996 Aug 23; 64(3):501-5. PubMed ID: 8862630
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  • 10. Interstitial 16q deletion with typical dysmorphic syndrome.
    Fryns JP, Proesmans W, Van Hoey G, Van den Berghe H.
    Ann Genet; 1981 Aug 23; 24(2):124-5. PubMed ID: 6977293
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  • 11. Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.
    Riegel M, Baumer A, Jamar M, Delbecque K, Herens C, Verloes A, Schinzel A.
    Hum Genet; 2001 Sep 23; 109(3):286-94. PubMed ID: 11702209
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  • 12. Ectrodactyly and proximal/intermediate interstitial deletion 7q.
    McElveen C, Carvajal MV, Moscatello D, Towner J, Lacassie Y.
    Am J Med Genet; 1995 Mar 13; 56(1):1-5. PubMed ID: 7747769
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  • 15. Tricho-rhino-phalangeal syndrome type I with severe mental retardation due to interstitial deletion of 8q23.3-24.13.
    Yamamoto Y, Oguro N, Miyao M, Yanagisawa M.
    Am J Med Genet; 1989 Jan 13; 32(1):133-5. PubMed ID: 2784939
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  • 17. Interstitial deletion of 8q13.3-->22.1 associated with craniosynostosis.
    Fryburg JS, Golden WL.
    Am J Med Genet; 1993 Mar 01; 45(5):638-41. PubMed ID: 7681252
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  • 19. Characterization of a 5.8-Mb interstitial deletion of chromosome 3p in a girl with 46,XX,inv(7)dn karyotype and phenotypic abnormalities.
    Morales C, Mademont-Soler I, Armengol L, Milà M, Badenas C, Andrés S, Soler A, Sánchez A.
    Cytogenet Genome Res; 2009 Mar 01; 125(4):334-40. PubMed ID: 19864897
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  • 20. 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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