Search Results - Anderlid, B.M.

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    Mutations in FLVCR2 associated with Fowler syndrome and survival beyond infancy

    Mutations in FLVCR2 associated with Fowler syndrome and survival beyond infancy by Kvarnung, M., Taylan, F., Nilsson, D., Albåge, M., Nordenskjöld, M., Anderlid, B.M., Nordgren, A., Syk Lundberg, E.

    Published in Clinical genetics
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