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Journal Abstract Search

141 related items for PubMed ID: 10588834

  • 1. De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype.
    Tihy F, Lemyre E, Lemieux N, Dallaire L.
    Am J Med Genet; 1999 Dec 03; 87(4):302-5. PubMed ID: 10588834
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  • 4. A patient with a de novo t (6;9) and an interstitial duplication of (9)(q21.2q22.1).
    Mohrschladt MF, Bijlsma EK, Sluijter S, De Coo RF, Hoovers JM, Leschot NJ.
    Clin Dysmorphol; 1999 Jul 03; 8(3):211-4. PubMed ID: 10457857
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  • 5. Xq chromosome duplication in males: clinical, cytogenetic and array CGH characterization of a new case and review.
    Cheng SF, Rauen KA, Pinkel D, Albertson DG, Cotter PD.
    Am J Med Genet A; 2005 Jun 15; 135(3):308-13. PubMed ID: 15887264
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  • 6. Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(X) (pter-->q24::q21.32-->qter) and random X inactivation.
    Carrozzo R, Arrigo G, Rossi E, Bardoni B, Cammarata M, Gandullia P, Gatti R, Zuffardi O.
    Am J Med Genet; 1997 Oct 31; 72(3):329-34. PubMed ID: 9332664
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  • 7. De novo duplication xq22-q23 in a girl with short stature and gonadal dysgenesis.
    Correa-Cerro L, Garcia-Cruz D, Ruiz MX, Sanchez-Corona J.
    Ann Genet; 1999 Oct 31; 42(1):41-4. PubMed ID: 10214506
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  • 12. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.
    Cappon SL, Duncan AM, Khalifa MM.
    Med Sci Monit; 2000 Oct 31; 6(3):581-5. PubMed ID: 11208374
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  • 14. De novo partial duplication of long arm of chromosome 13: dup(13)(q12-->q14).
    Hermann R, Soltész G, Morava E, Kosztolányi G, Czakó M.
    Am J Med Genet; 2000 Jun 05; 92(4):296-7. PubMed ID: 10842301
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  • 16. De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?
    Redha MA, Krishna Murthy DS, al-Awadi SA, al-Sulaiman IS, Sabry MA, el-Bahey SA, Farag TI.
    Ann Genet; 1996 Jun 05; 39(1):5-9. PubMed ID: 9297445
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  • 17. FISH analysis for apparently simple terminal deletions of the X chromosome: identification of hidden structural abnormalities.
    Ogata T, Matsuo N, Fukushima Y, Saito M, Nose O, Miharu N, Uehara S, Ishizuka B.
    Am J Med Genet; 2001 Dec 15; 104(4):307-11. PubMed ID: 11754066
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  • 19. De novo dup(X)(q22.3q26) in a girl with evidence that functional disomy of X material is the cause of her abnormal phenotype.
    Armstrong L, McGowan-Jordan J, Brierley K, Allanson JE.
    Am J Med Genet A; 2003 Jan 01; 116A(1):71-6. PubMed ID: 12476455
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