Characterisation of a microdeletion in Xp11.23 cosegregating in a small family with X-linked retinitis pigmentosa (RP2) and psychosis.

Thiselton, DL;Brandau, O;Meindl, A;Riley, BP;Hardcastle, AJ;et.al.
(2002) 52nd Annual Meeting of the American-Society-of-Human-Genetics — Location: BALTIMORE(Maryland) (15.October.2002)

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  • Thiselton, DL
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  • Brandau, O
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  • Meindl, A
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  • Riley, BP
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  • Hardcastle, AJ
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Thiselton, D., Brandau, O., Meindl, A., Riley, B., Kendler, K., Van Maldergem, L., & Hardcastle, A. (2002). Characterisation of a microdeletion in Xp11.23 cosegregating in a small family with X-linked retinitis pigmentosa (RP2) and psychosis. American Journal of Human Genetics, 71(4), 508. https://hdl.handle.net/2078.5/141733 (Original work published 2002)