A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation
Criteria of the German Consortium for Hereditary Breast and Ovarian Cancer for the Classification of Germline Sequence Variants
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Clinical exome sequencing in earlyâ•'onset generalized dystonia and largeâ•'scale resequencing followâ•'up
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Alfons Meindl's research works | Ludwig-Maximilians-University of Munich, München (LMU) and other places
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