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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

329 related items for PubMed ID: 4795737

  • 1.
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  • 2. Malformative syndrome with ring chromosome 13.
    Fryns JP, Deoover J, Van den Berghe H.
    Humangenetik; 1974; 24(3):235-40. PubMed ID: 4140834
    [No Abstract] [Full Text] [Related]

  • 3. Syndrome associated with group-D chromosome deletions.
    Lehrke R, Thelen T, Lehrke R.
    Lancet; 1971 Jul 10; 2(7715):98-9. PubMed ID: 4104010
    [No Abstract] [Full Text] [Related]

  • 4. A case of a girl with a 21 ring chromosome.
    Kucerová M, Polívková Z.
    Hum Hered; 1974 Jul 10; 24(1):100-4. PubMed ID: 4136482
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  • 6. Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.
    Sanchez O, Yunis JJ, Escobar JI.
    Humangenetik; 1974 Apr 24; 22(1):59-65. PubMed ID: 4134840
    [No Abstract] [Full Text] [Related]

  • 7. [A single D chromosome in ring form in a 2-year-old girl with mental retardation].
    Morić-Petrović S, Garzicić B, Despotović M, Kalicanin P.
    Srp Arh Celok Lek; 1970 Mar 24; 98(3):447-52. PubMed ID: 5205520
    [No Abstract] [Full Text] [Related]

  • 8. Ring chromosome 6: case report and review of literature.
    Kini KR, Van Dyke DL, Weiss L, Logan MS.
    Hum Genet; 1979 Mar 24; 50(2):145-9. PubMed ID: 511129
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  • 12. [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
    Rethoré MO, Hoehn H, Rott HD, Couturier J, Dutrillaux B, Lejeune J.
    Humangenetik; 1973 Apr 16; 18(2):129-38. PubMed ID: 4124236
    [No Abstract] [Full Text] [Related]

  • 13. "Cri du chat" syndrome with maternal insertional translocation.
    Berger R, Touati G, Derre J, Ortiz MA, Martinetti J.
    Clin Genet; 1974 Apr 16; 5(5):428-32. PubMed ID: 4368036
    [No Abstract] [Full Text] [Related]

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  • 15. A case of D13 ring chromosome.
    Cossu P, Diana G, Mameli M, Cardia S, Milia A, Floris G, Cao A.
    Hum Genet; 1979 Jan 19; 46(1):111-4. PubMed ID: 429001
    [Abstract] [Full Text] [Related]

  • 16. A terminal deletion (14)(q31.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and mild mental retardation.
    Yen FS, Podruch PE, Weisskopf B.
    J Med Genet; 1989 Feb 19; 26(2):130-3. PubMed ID: 2918542
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  • 18. Tandem duplication (5q13 to 22) in a mentally deficient girl.
    Kessel E, Pfeiffer RA.
    Hum Genet; 1979 Nov 19; 52(2):217-20. PubMed ID: 511177
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