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Journal Abstract Search

186 related items for PubMed ID: 8651261

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  • 2. Maternal disomy and Prader-Willi syndrome consistent with gamete complementation in a case of familial translocation (3;15) (p25;q11.2).
    Park JP, Moeschler JB, Hani VH, Hawk AB, Belloni DR, Noll WW, Mohandas TK.
    Am J Med Genet; 1998 Jun 30; 78(2):134-9. PubMed ID: 9674903
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  • 3. Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.
    Mutirangura A, Greenberg F, Butler MG, Malcolm S, Nicholls RD, Chakravarti A, Ledbetter DH.
    Hum Mol Genet; 1993 Feb 30; 2(2):143-51. PubMed ID: 8499903
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  • 4. Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome.
    Fridman C, Koiffmann CP.
    Am J Med Genet; 2000 Sep 18; 94(3):249-53. PubMed ID: 10995513
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  • 9. Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation.
    Calounova G, Novotna D, Simandlova M, Havlovicova M, Zumrová A, Kocarek E, Sedlacek Z.
    Neuro Endocrinol Lett; 2006 Oct 18; 27(5):579-85. PubMed ID: 17159828
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  • 10. Why is there no diploid overdose effect in Prader-Willi syndrome due to uniparental disomy?
    Smith A.
    Acta Genet Med Gemellol (Roma); 1996 Oct 18; 45(1-2):179-89. PubMed ID: 8872029
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  • 14. Prader-Willi syndrome and Tay-Sachs disease in association with mixed maternal uniparental isodisomy and heterodisomy 15 in a girl who also had isochromosome Xq.
    Zeesman S, McCready E, Sadikovic B, Nowaczyk MJ.
    Am J Med Genet A; 2015 Jan 18; 167A(1):180-4. PubMed ID: 25287655
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  • 15. Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method.
    Zeschnigk M, Schmitz B, Dittrich B, Buiting K, Horsthemke B, Doerfler W.
    Hum Mol Genet; 1997 Mar 18; 6(3):387-95. PubMed ID: 9147641
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  • 17. Complex rearrangements of chromosome 15 in two patients with mild/atypical Prader Willi syndrome.
    Salavoura K, Kolialexi A, Sofocleous C, Kalaitzidaki M, Pampanos A, Kitsiou S, Mavrou A.
    Genet Couns; 2008 Mar 18; 19(2):219-24. PubMed ID: 18618997
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