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Journal Abstract Search

170 related items for PubMed ID: 1139790

  • 1. Ring chromosome 13 syndrome.
    Fried K, Rosenblatt M, Mundel G, Krikler R.
    Clin Genet; 1975 Mar; 7(3):203-8. PubMed ID: 1139790
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  • 3. Ring chromosome 6: case report and review of literature.
    Kini KR, Van Dyke DL, Weiss L, Logan MS.
    Hum Genet; 1979 Mar; 50(2):145-9. PubMed ID: 511129
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  • 5. Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).
    Schinzel A, Hayashi K, Schmid W.
    Humangenetik; 1975 Dec 23; 30(4):307-16. PubMed ID: 1218860
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  • 6. Ring chromosome 14: a distinct clinical entity.
    Schmidt R, Eviatar L, Nitowsky HM, Wong M, Miranda S.
    J Med Genet; 1981 Aug 23; 18(4):304-7. PubMed ID: 7277427
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  • 7. Developmental abnormalities associated with a ring chromosome 6.
    Moore CM, Heller RH, Thomas GH.
    J Med Genet; 1973 Sep 23; 10(3):299-303. PubMed ID: 4774541
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  • 11. A case of a girl with a 21 ring chromosome.
    Kucerová M, Polívková Z.
    Hum Hered; 1974 Sep 23; 24(1):100-4. PubMed ID: 4136482
    [No Abstract] [Full Text] [Related]

  • 12. A de novo 4.4-Mb microdeletion in 2p24.3 → p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome.
    Chen CP, Lin SP, Chern SR, Wu PS, Chang SD, Ng SH, Liu YP, Su JW, Wang W.
    Eur J Med Genet; 2012 Nov 23; 55(11):666-9. PubMed ID: 22842076
    [Abstract] [Full Text] [Related]

  • 13. Malformative syndrome with ring chromosome 13.
    Fryns JP, Deoover J, Van den Berghe H.
    Humangenetik; 1974 Nov 23; 24(3):235-40. PubMed ID: 4140834
    [No Abstract] [Full Text] [Related]

  • 14. Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.
    Podruch PE, Weisskopf B.
    J Pediatr; 1974 Jul 23; 85(1):92-5. PubMed ID: 4855265
    [No Abstract] [Full Text] [Related]

  • 15. Ring-G chromosome, a new G-deletion syndrome?
    Weleber RG, Hecht F, Giblett ER.
    Am J Dis Child; 1968 Apr 23; 115(4):489-93. PubMed ID: 4296014
    [No Abstract] [Full Text] [Related]

  • 16. [Ring chromosome 14. II. A case report of r(14) mosaicism. The r(14) phenotype].
    Rethoré MO, Caille B, Huet de Barochez Y, de Blois MC, Ravel A, Lejeune J.
    Ann Genet; 1984 Apr 23; 27(2):91-5. PubMed ID: 6331796
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  • 17. An unexpected finding in a child with neurological problems: mosaic ring chromosome 18.
    Koç A, Kan D, Karaer K, Ergün MA, Karaoğuz MY, Gücüyener K, Hinreiner S, Liehr T, Perçin EF.
    Eur J Pediatr; 2008 Jun 23; 167(6):655-9. PubMed ID: 17668239
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  • 18. 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 23; 26(2):130-3. PubMed ID: 2918542
    [Abstract] [Full Text] [Related]

  • 19. The 4p-syndrome, with a report of two new cases.
    Fryns JP, Eggermont E, Verresen H, Van den Berghe H.
    Humangenetik; 1973 Feb 23; 19(1):99-109. PubMed ID: 4725911
    [No Abstract] [Full Text] [Related]

  • 20. Screening for autosomal aberrations.
    Higurashi M, Segawa M, Matsui I, Ihnuma K, Nakagome Y.
    Acta Paediatr Scand; 1977 Jul 23; 66(4):501-4. PubMed ID: 899767
    [Abstract] [Full Text] [Related]

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