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Journal Abstract Search

166 related items for PubMed ID: 6723106

  • 41. Partial trisomy for the short arm of chromosome 2 due to familial balance translocation.
    Sekhon GS, Taysi K, Rath R.
    Hum Genet; 1978 Oct 19; 44(1):99-103. PubMed ID: 711241
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  • 43. Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-).
    Penehaszadeh VB, Coco R.
    J Med Genet; 1975 Sep 19; 12(3):301-5. PubMed ID: 1177284
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  • 51. Familial partial trisomy of the long arm of chromosome 10 (q24-26).
    Moreno-Fuenmayor H, Zackai EH, Mellman WJ, Aronson M.
    Pediatrics; 1975 Nov 19; 56(5):756-61. PubMed ID: 1196732
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  • 52. [Partial trisomy of the long arm of chromosome 2 by malsegregation of a maternal translocation t(2;7)(q321;p22)].
    Siffroi JP, Romani F, Viguié F, Lejeune C.
    Ann Genet; 1984 Nov 19; 27(4):241-4. PubMed ID: 6335372
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  • 53. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.
    Butler LJ, Eades SM, France NE.
    Ann Genet; 1969 Mar 19; 12(1):15-27. PubMed ID: 5306708
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  • 54. Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother.
    Hobolth N, Jacobsen P, Mikkelsen M.
    J Med Genet; 1974 Sep 19; 11(3):299-303. PubMed ID: 4139263
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  • 55. Malformation syndrome of duplication 12q24.1 leads to qter.
    Melnyk AR, Weiss L, Van Dyke DL, Jarvi P.
    Am J Med Genet; 1981 Sep 19; 10(4):357-65. PubMed ID: 7332029
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  • 56. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
    Frankova YE, Holenova H, Braulke I.
    Monatsschr Kinderheilkd; 1991 Dec 19; 139(12):841-3. PubMed ID: 1770961
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  • 58. 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 19; 18(2):99-103. PubMed ID: 1081372
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  • 59. A malformed girl with duplication of chromosome 9q.
    Nakahori Y, Nakagome Y.
    J Med Genet; 1984 Oct 19; 21(5):387-8. PubMed ID: 6502654
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  • 60. Phenotype of partial trisomy 8 (p21 leads to qter) in two unrelated patients with de novo translocation.
    Sachs ES, van Waveren G.
    J Med Genet; 1981 Jun 19; 18(3):204-8. PubMed ID: 7241543
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