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Journal Abstract Search

193 related items for PubMed ID: 7358385

  • 1. Balanced translocation (10;13) in a father, ascertained through the study of meiosis in semen, and partial trisomy 10q in his son. Characterization of the region responsible for the partial trisomy 10q syndrome.
    Miró R, Templado C, Ponsá M, Serradell J, Marina S, Egozcue J.
    Hum Genet; 1980 Feb; 53(2):179-82. PubMed ID: 7358385
    [Abstract] [Full Text] [Related]

  • 2. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS, Kamel AK, Helmy NA.
    Genet Couns; 2008 Feb; 19(2):199-209. PubMed ID: 18618995
    [Abstract] [Full Text] [Related]

  • 3. Partial trisomy 10q: a recognizable syndrome.
    Klep-de Pater JM, Bijlsma JB, de France HF, Leschot NJ, Duijndam-van den Berge M, van Hemel JO.
    Hum Genet; 1979 Jan 19; 46(1):29-40. PubMed ID: 429004
    [Abstract] [Full Text] [Related]

  • 4. A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter.
    Voss R, Gross-Kieselstein E, Hurvitz H, Dagan J, Kerem E, Zlotogora J.
    J Med Genet; 1984 Dec 19; 21(6):454-9. PubMed ID: 6512835
    [Abstract] [Full Text] [Related]

  • 5. A severely retarded 18-year-old boy with tertiary partial trisomy 14.
    Smith A, den Dulk G, Elliott G.
    J Med Genet; 1980 Jun 19; 17(3):230-2. PubMed ID: 7401136
    [Abstract] [Full Text] [Related]

  • 6. 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 19; 28(3):193-6. PubMed ID: 3879157
    [Abstract] [Full Text] [Related]

  • 7. Partial trisomy 10q occurring in a family with a reciprocal translocation t(10;18)(q25;q23).
    Kroyer S, Niebuhr E.
    Ann Genet; 1975 Mar 19; 18(1):50-5. PubMed ID: 50043
    [Abstract] [Full Text] [Related]

  • 8. Partial trisomy 13 with phenotype of Patau syndrome due to maternal reciprocal translocation t(6;13) (q25;q13).
    Petit P, Fryns JP, van den Berghe H.
    Ann Genet; 1980 Mar 19; 23(1):57-9. PubMed ID: 6965845
    [No Abstract] [Full Text] [Related]

  • 9. 'Pure' partial trisomy 2q in a male owing to malsegregation of a maternal translocation t(X;2)(p22.3;q32.1).
    Plessis G, Couturier J, Turleau C, Despoisses S, Delavenne J.
    J Med Genet; 1985 Feb 19; 22(1):70-3. PubMed ID: 3981584
    [Abstract] [Full Text] [Related]

  • 10. Partial trisomy for the long arm of chromosome 7 due to familial balanced translocation.
    Schmid M, Wolf J, Nestler H, Krone W.
    Hum Genet; 1979 Jul 18; 49(3):283-9. PubMed ID: 478537
    [Abstract] [Full Text] [Related]

  • 11. Tertiary trisomy 14q--, due to paternal balanced translocation 46,XY,t(1;14)(q44;q22).
    Kovacs G, Mihai C.
    Hum Genet; 1979 Jun 19; 49(2):175-8. PubMed ID: 468247
    [Abstract] [Full Text] [Related]

  • 12. Unbalanced karyotype with normal phenotype in a family with translocation (8;13)(p21;q22).
    Bröcker-Vriends AH, van de Kamp JJ, Geraedts JP, Bos SE, Nijenhuis TA.
    Clin Genet; 1985 May 19; 27(5):487-95. PubMed ID: 4006274
    [Abstract] [Full Text] [Related]

  • 13. [Partial "de novo" trisomy 10q (author's transl)].
    Berger R, Derre J, Murawsky M, Amiel-Tison C.
    J Genet Hum; 1976 Dec 19; 24(4):261-9. PubMed ID: 1022850
    [Abstract] [Full Text] [Related]

  • 14. Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.
    Lindenbaum RH, Bobrow M.
    J Med Genet; 1975 Mar 19; 12(1):29-43. PubMed ID: 123589
    [Abstract] [Full Text] [Related]

  • 15. Partial trisomy 12q: report of a case and review.
    Roberts SH, Mattina T, Laurence KM, Sorge G, Pavone L.
    J Med Genet; 1981 Dec 19; 18(6):470-3. PubMed ID: 7334509
    [Abstract] [Full Text] [Related]

  • 16. [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 19; 17(2):125-9. PubMed ID: 7149479
    [Abstract] [Full Text] [Related]

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  • 18. Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3).
    van de Vooren MJ, Planteydt HT, Hagemeijer A, Peters-Slough MF, Timmerman MJ.
    Clin Genet; 1984 Jan 19; 25(1):52-8. PubMed ID: 6705241
    [Abstract] [Full Text] [Related]

  • 19. Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and delection 10q.
    Larson LM, Wasdahl WA, Saumur JH, Coleman ML, Hall JG, Dolan CR, Schutta CJ.
    Clin Genet; 1982 Mar 19; 21(3):187-95. PubMed ID: 7094394
    [Abstract] [Full Text] [Related]

  • 20. Partial trisomy 6p and partial trisomy 22 resulting from 3:1 meiotic disjunction of maternal (6p;22q) translocation.
    Scarbrough PR, Carroll AJ, Finley SC, Hamerick K.
    J Med Genet; 1986 Apr 19; 23(2):185-7. PubMed ID: 3712400
    [Abstract] [Full Text] [Related]

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