Works matching IS 09646906 AND DT 2004 AND VI 13 AND IP 4


Results: 11
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    Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion.

    Published in:
    Human Molecular Genetics, 2004, v. 13, n. 4, p. 417, doi. 10.1093/hmg/ddh041
    By:
    • Saitta, Sulagna C.;
    • Harris, Stacy E.;
    • Gaeth, Ann P.;
    • Driscoll, Deborah A.;
    • McDonald-McGinn, Donna M.;
    • Maisenbacher, Melissa K.;
    • Yersak, Jill M.;
    • Chakraborty, Prabir K.;
    • Hacker, April M.;
    • Zackai, Elaine H.;
    • Ashley, Terry;
    • Emanuel, Beverly S.
    Publication type:
    Article
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