登入選單
返回Google圖書搜尋
A Homozygous Deletion of Exon 5 of KYNU Resulting from a Maternal Chromosome 2 Isodisomy (UPD2) Causes Catel-Manzke-Syndrome/VCRL Syndrome
Isabel SchüleUrs BergerUta MatysiakGunda RuzaikeBrigitte StillerMartin PohlUte SpiekerkötterEkkehart LauschSarah GrünertMiriam Schmidts
出版Universität, 2021
URLhttp://books.google.com.hk/books?id=6jV0zwEACAAJ&hl=&source=gbs_api