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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

118 related items for PubMed ID: 9001808

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  • 4. Emanuel syndrome due to unusual segregation of paternal origin.
    Zaki MS, Mohamed AM, Kamel AK, El-Gerzawy AM, El-Ruby MO.
    Genet Couns; 2012; 23(2):319-28. PubMed ID: 22876593
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  • 6. [Familial chromosome translocation (1;5;15) as a cause of partial trisomy 1p].
    Schürmann M, Wethling H, Niemeyer ML, Schwinger E.
    Klin Padiatr; 1987; 199(1):27-31. PubMed ID: 2435950
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  • 7. Tissue limited mosaicism for unbalanced autosomal translocation in a child with congenital anomalies and mental retardation.
    Summitt RL, Tharapel AT, Wilroy RS.
    Eur J Pediatr; 1977 Jul 01; 125(3):169-74. PubMed ID: 885143
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  • 10. Cerebro-oculo-facio-skeletal (COFS) syndrome in siblings.
    Kulkarni ML, Sehgal A, Keshavamurthy KS, Kulkarni PM.
    Indian J Pediatr; 2004 Dec 01; 71(12):e56-7. PubMed ID: 15630331
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  • 15. Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy.
    Schinzel A, Kotzot D, Brecevic L, Robinson WP, Dutly F, Dauwerse H, Binkert F, Baumer A, Ausserer B.
    Eur J Hum Genet; 1997 Dec 01; 5(5):308-14. PubMed ID: 9412788
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  • 17. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
    Qumsiyeh MB, Stevens CA.
    Am J Med Genet; 1993 Sep 01; 47(3):387-91. PubMed ID: 8135287
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  • 18. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].
    Giovannelli G, Forabosco A, Dutrillaux B.
    Ann Genet; 1974 Jun 01; 17(2):119-24. PubMed ID: 4547939
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