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PUBMED FOR HANDHELDS

Journal Abstract Search

288 related items for PubMed ID: 8135281

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  • 22. Novel isodicentric chromosome 18 in an abnormal infant with a mosaic karyotype [46,XY/46,XY,-18,+dic(18)(q12.2]).
    Bryke CR, Lindgren V, Fryburg JS, Yang-Feng TL.
    Am J Med Genet; 1990 Jun; 36(2):247-50. PubMed ID: 2368814
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  • 26. Pregnancy outcome following prenatal diagnosis of an isodicentric X chromosome: first case report.
    Lebbar A, Viot G, Szpiro-Tapia S, Baverel F, Rabineau D, Dupont JM.
    Prenat Diagn; 2002 Nov; 22(11):973-5. PubMed ID: 12424758
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  • 30. Dir dup(X) (q13-->qter) in a girl with growth retardation, microcephaly, developmental delay, seizures, and minor anomalies.
    Aughton DJ, AlSaadi AA, Johnson JA, Transue DJ, Trock GL.
    Am J Med Genet; 1993 Apr 15; 46(2):159-64. PubMed ID: 7683452
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  • 33. Ring chromosome 2 in a child with growth failure and few congenital abnormalities.
    Vigfusson NV, Kapstafer KJ, Lloyd MA.
    Am J Med Genet; 1980 Apr 15; 7(3):383-9. PubMed ID: 7468662
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  • 37. Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome.
    Urioste M, Visedo G, Sanchís A, Sentís C, Villa A, Ludeña P, Hortigüela JL, Martínez-Frías ML, Fernández-Piqueras J.
    Am J Med Genet; 1994 Jan 01; 49(1):77-82. PubMed ID: 8172255
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  • 38. Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication study.
    Stavropoulou C, Mignon C, Delobel B, Moncla A, Depetris D, Croquette MF, Mattei MG.
    J Med Genet; 1998 Nov 01; 35(11):932-8. PubMed ID: 9832041
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