Fluorescence in-situ hybridisation and molecular studies used in the characterisation of a Robertsonian translocation (13q15q) in Prader-Willi syndrome
(Q40891413)
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Fluorescence in-situ hybridisation and molecular studies used in the characterisation of a Robertsonian translocation (13q15q) in Prader-Willi syndrome
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External Links
(P356) |
10.1111/J.1399-0004.1993.TB04416.X
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(P698) |
8462197
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