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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
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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
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3
Hereditary Prosopagnosia: the First Case Series
Grueter, M.
;
Grueter, T.
;
Bell, Vaughan
. - : Elsevier, 2007
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