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24. Genetics. The critical region in trisomy 21. Nelson DL; Gibbs RA Science; 2004 Oct; 306(5696):619-21. PubMed ID: 15499000 [No Abstract] [Full Text] [Related]
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27. Partial trisomy of chromosome 21 without the Down syndrome phenotype. Su MT; Kuan LC; Chou YY; Tan SY; Kuo TC; Kuo PL Prenat Diagn; 2016 May; 36(5):492-5. PubMed ID: 26918398 [No Abstract] [Full Text] [Related]
28. Assignment of three human markers in chromosome 21q11 to mouse chromosome 16. Yu J; Shen Y; Tong S; Kao FT Somat Cell Mol Genet; 1997 Sep; 23(5):367-70. PubMed ID: 9546078 [TBL] [Abstract][Full Text] [Related]
29. Down syndrome and the genes of human chromosome 21: current knowledge and future potentials. Report on the Expert workshop on the biology of chromosome 21 genes: towards gene-phenotype correlations in Down syndrome. Washington D.C., September 28-October 1, 2007. Pritchard M; Reeves RH; Dierssen M; Patterson D; Gardiner KJ Cytogenet Genome Res; 2008; 121(1):67-77. PubMed ID: 18544929 [TBL] [Abstract][Full Text] [Related]
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32. [Genome analysis of human chromosome 21: transcript mapping of the Down syndrome region]. Ohira M; Ohki M Seikagaku; 1997 Apr; 69(4):229-43. PubMed ID: 9168674 [No Abstract] [Full Text] [Related]
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40. Down syndrome genetics: unravelling a multifactorial disorder. Hernandez D; Fisher EM Hum Mol Genet; 1996; 5 Spec No():1411-6. PubMed ID: 8875245 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]