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Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder
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| Author |
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| Abstract |
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| Language |
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English
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| Source (journal) |
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Human mutation. - New York, N.Y. |
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| Publication |
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New York, N.Y. : 2012
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| ISSN |
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1059-7794
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| Volume/pages |
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33:11(2012), p. 1599-1609
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| ISI |
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000309755800013
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| Full text (Publisher's DOI) |
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