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Journal Abstract Search

196 related items for PubMed ID: 7802006

  • 1. Duplication 10q confirmed by DNA in situ hybridization.
    Johnson VP, Sutliff WC.
    Am J Med Genet; 1994 Aug 15; 52(2):184-7. PubMed ID: 7802006
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  • 2. Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.
    Fryns JP, Kleczkowska A, Kenis H, Decock P, Van den Berghe H.
    Ann Genet; 1989 Aug 15; 32(3):174-6. PubMed ID: 2573314
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  • 3. Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence.
    Lindgren V, Rosinsky B, Chin J, Berry-Kravis E.
    Am J Med Genet; 1994 Jan 01; 49(1):67-73. PubMed ID: 8172253
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  • 6. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
    van Buggenhout G, Decock P, Fryns JP.
    Genet Couns; 1996 Jan 01; 7(1):53-9. PubMed ID: 8652089
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  • 9. [Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].
    Aledo AG, Gracia R, López Pajares I, González M, Oliver A, Peralta A.
    An Esp Pediatr; 1982 Aug 01; 17(2):125-9. PubMed ID: 7149479
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  • 12. Familial partial duplication (1)(p21p31).
    Hoechstetter L, Soukup S, Schorry EK.
    Am J Med Genet; 1995 Nov 20; 59(3):291-4. PubMed ID: 8599351
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  • 13. Delineation of a duplication map of chromosome 3q: a new case confirms the exclusion of 3q25-q26.2 from the duplication 3q syndrome critical region.
    Rizzu P, Haddad BR, Vallcorba I, Alonso A, Ferro MT, Garcia-Sagredo JM, Baldini A.
    Am J Med Genet; 1997 Feb 11; 68(4):428-32. PubMed ID: 9021016
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  • 14. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC, Carnevale A, Gómez L, del Castillo V, Frías S.
    Rev Invest Clin; 1996 Feb 11; 48(1):27-33. PubMed ID: 8815483
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  • 15. Apparent CHARGE association and chromosome anomaly: chance or contiguous gene syndrome.
    Clementi M, Tenconi R, Turolla L, Silvan C, Bortotto L, Artifoni L.
    Am J Med Genet; 1991 Nov 01; 41(2):246-50. PubMed ID: 1785643
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  • 16. Four new cases of inverted terminal duplication: a modified hypothesis of mechanism of origin.
    Hoo JJ, Chao M, Szego K, Rauer M, Echiverri SC, Harris C.
    Am J Med Genet; 1995 Sep 25; 58(4):299-304. PubMed ID: 8533837
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  • 17. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS, Kamel AK, Helmy NA.
    Genet Couns; 2008 Sep 25; 19(2):199-209. PubMed ID: 18618995
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  • 18. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
    Bhat M, Morrison PJ, Getty A, McManus D, Tubman R, Nevin NC.
    Am J Med Genet; 2000 Mar 20; 91(3):201-3. PubMed ID: 10756343
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  • 19. Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13).
    Tschernigg M, Petek E, Leonhardtsberger A, Wagner K, Kroisel PM.
    Genet Couns; 2002 Mar 20; 13(3):303-7. PubMed ID: 12416638
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