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Journal Abstract Search

150 related items for PubMed ID: 3378367

  • 1.
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  • 2. Multiple critical smallest region of overlap in monosomy 16Q syndrome?
    Doco-Fenzy M, Elchardus JF, Brami G, Digeon B, Gruson N, Adnet JJ.
    Genet Couns; 1994; 5(1):39-44. PubMed ID: 8031534
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  • 4. Interstitial deletion and ring chromosome derived from 16q.
    Krauss CM, Caldwell D, Atkins L.
    J Med Genet; 1987 May; 24(5):308-12. PubMed ID: 3585948
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  • 5. Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features.
    Trautmann U, Pfeiffer RA, Seufert-Satomi U, Tietze HU.
    J Med Genet; 1993 Apr; 30(4):330-1. PubMed ID: 8487285
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  • 6. Ring chromosome 16: a new case.
    Vianello MG, Cottafava F, Bartoli D, Franzone G, Casazzava R, Gastaldi R.
    Ann Genet; 1990 Apr; 33(1):36-9. PubMed ID: 2195979
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  • 8. Duplication 16q12----qter arising from 3:1 segregation in a 46,XX,t(13;16) (q12;q12) mother.
    Pérez-Castillo A, Martin-Lucas MA, Abrisqueta JA.
    Ann Genet; 1990 Apr; 33(2):121-3. PubMed ID: 2241087
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  • 9. Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: clinical description of a new patient.
    Caliebe A, Waltz S, Jenderny J.
    Clin Genet; 1997 Aug; 52(2):116-9. PubMed ID: 9298747
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  • 10. Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46,XX,del(2)(q31q33).
    Benson K, Gordon M, Wassman ER, Tsi C.
    Am J Med Genet; 1986 Nov; 25(3):405-11. PubMed ID: 3789004
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  • 11. Interstitial deletion of the band 4p15.3 defined by sequential replication banding.
    Davies J, Voullaire L, Bankier A.
    Ann Genet; 1990 Nov; 33(2):92-5. PubMed ID: 2241091
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  • 12. High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.
    Callen DF, Eyre H, Lane S, Shen Y, Hansmann I, Spinner N, Zackai E, McDonald-McGinn D, Schuffenhauer S, Wauters J.
    J Med Genet; 1993 Oct; 30(10):828-32. PubMed ID: 8230159
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  • 15. Identical twins with deletion 16q syndrome: evidence that 16q12.2-q13 is the critical band region.
    Elder FF, Ferguson JW, Lockhart LH.
    Hum Genet; 1984 Oct; 67(2):233-6. PubMed ID: 6540242
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  • 17. Langer-Giedion syndrome with interstitial 8q-deletion.
    Zabel BU, Baumann WA.
    Am J Med Genet; 1982 Mar; 11(3):353-8. PubMed ID: 7081298
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  • 19. A girl with an interstitial deletion of the short arm of chromosome 3 studied with a high-resolution banding technique.
    Sichong Z, Bui TH, Castro I, Iselius L, Håkansson S, Lundmark KM.
    Hum Genet; 1981 Mar; 59(2):178-81. PubMed ID: 7327578
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  • 20. Terminal deletion of the short arm of chromosome 3.
    Lizcano-Gil LA, Figuera LE.
    Genet Couns; 1994 Mar; 5(1):35-8. PubMed ID: 8031533
    [Abstract] [Full Text] [Related]

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