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Journal Abstract Search

833 related items for PubMed ID: 7102721

  • 1. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
    Voss R, Lerer I, Maftzir G, Sheinis M, Cohen MM.
    Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721
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  • 2. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
    Ito M, Mutoh K, Okuno T, Mikawa H, Edagawa J, Abe T.
    Ann Genet; 1983 Jun; 26(2):116-9. PubMed ID: 6604486
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  • 3. Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.
    García-Cruz D, García-Esquivel L, Rivera H, Vaca G, Rolón A, Cantú JM.
    Ann Genet; 1985 Jun; 28(3):193-6. PubMed ID: 3879157
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  • 4. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J, Plaza J, Geán E.
    An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
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  • 5. Trisomy 9 mosaicism in a girl with multiple malformations.
    Diaz-Mares L, Molina B, Carnevale A.
    Ann Genet; 1990 Nov; 33(3):165-8. PubMed ID: 2288462
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  • 6. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
    Chen H, Tuck-Muller CM, Batista DA, Wertelecki W.
    Am J Med Genet; 1995 Mar 27; 56(2):219-33. PubMed ID: 7625449
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  • 7. 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 Mar 27; 32(3):174-6. PubMed ID: 2573314
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  • 10. Partial trisomy 15q: report of a patient and literature review.
    Chandler K, Schrander-Stumpel CT, Engelen J, Theunissen P, Fryns JP.
    Genet Couns; 1997 Mar 27; 8(2):91-7. PubMed ID: 9219006
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  • 11. Secondary trisomy or mosaic "tetrasomy" 8p.
    Robinow M, Haney N, Chen H, Sorauf T, Van Dyke DL, Babu VR, Powell S, Maliszewski W, Guerin S, Landers JW.
    Am J Med Genet; 1989 Mar 27; 32(3):320-4. PubMed ID: 2729351
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  • 12. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].
    Giovannelli G, Forabosco A, Dutrillaux B.
    Ann Genet; 1974 Jun 27; 17(2):119-24. PubMed ID: 4547939
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  • 15. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
    Cohen MM, Ornoy A, Rosenmann A, Kohn G.
    Ann Genet; 1975 Jun 27; 18(2):99-103. PubMed ID: 1081372
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  • 16. Partial trisomy 20 confirmed by gene dosage studies.
    Rudd NL, Bain HW, Giblett E, Chen SH, Worton RG.
    Am J Med Genet; 1979 Jun 27; 4(4):357-64. PubMed ID: 231907
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  • 19. [Postaxial polydactyly: a symptom of partial trisomy of the long arm of chromosome 13. Two new observations with 46, XX, t (22;13) (q13;q31) and 46, XY, Dup (13) (pter-q34::q22-qter) (author's transl)].
    Kessel E, Pfeiffer RA, Baisch C.
    Klin Padiatr; 1980 Jan 27; 192(1):85-90. PubMed ID: 7188997
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