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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Hits 1 – 3 of 3 1 Extreme founder effect associated with oculocutaneous albinism type 1 (OCA1) on the island of Nias/Indonesia:How clinical genetics may help population genetics Kennerknecht, I. (Ingo); Zühlke, C. (Christine); Hämmerle, J.M. (Johannes). - 2021 BASE Show details 2 Klinik des 5p-minus Syndroms (syn. Cri-du-Chat Syndrom):Daten einer Fragebogenerhebung (2010 – 2019) Kennerknecht, I. (Ingo); Kröll-Schulte, A. (Agnes); Schulte, H.R. (Hans). - 2021 BASE Show details 3 Hereditary Prosopagnosia: the First Case Series Grueter, M.; Grueter, T.; Bell, Vaughan. - : Elsevier, 2007 BASE Show details

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