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  1. Mutation screening in Borjeson-Forssman-Lehmann syndrome: identification of a novel de...

    BACKGROUND: Borjeson-Forssman-Lehmann syndrome (BFLS; MIM 301900) is an infrequently described X linked disorder caused by mutations in PHF6, a novel zinc finger gene of unknown function. OBJECTIVE: To present the results of mutation screening in

    http://iris.ucl.ac.uk/iris/publication/72682/1

  2. Mutation screening in Borjeson-Forssman-Lehmann Syndrome (BFLS): Identification of a...

    BACKGROUND: Borjeson-Forssman-Lehmann syndrome (BFLS; MIM 301900) is an infrequently described X-linked disorder of intellectual disability, characteristic craniofacial features, microcephaly, hypogonadism, obesity, short stature and epilepsy,

    http://iris.ucl.ac.uk/iris/publication/68265/1

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