The parental origin and chromosomal mechanism for duplication 17p11.2 - the reciprocal recombination product of deletion 17p11.2 associated with Smith-Magenis syndrome.
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Park, SS
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机构:Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
Park, SS
Chen, KS
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机构:Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
Chen, KS
Potocki, L
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机构:Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
Potocki, L
Lupski, JR
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机构:Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
Lupski, JR
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[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
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Univ Calif San Francisco, Dept Pediat, Div Genet, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Pediat, Div Genet, San Francisco, CA 94143 USA
Sanford, E. F.
Bermudez-Wagner, K.
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Univ Calif San Francisco, Dept Pediat, Div Genet, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Pediat, Div Genet, San Francisco, CA 94143 USA
Bermudez-Wagner, K.
Jeng, L. J. B.
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Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Pediat, Div Genet, San Francisco, CA 94143 USA
Jeng, L. J. B.
Rauen, K. A.
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Univ Calif San Francisco, Dept Pediat, Div Genet, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Pediat, Div Genet, San Francisco, CA 94143 USA
Rauen, K. A.
Slavotinek, Anne M.
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Univ Calif San Francisco, Dept Pediat, Div Genet, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Pediat, Div Genet, San Francisco, CA 94143 USA