檢索結果 - Axelsen, Michael

  • Showing 1 - 3 results of 3
Refine Results
  1. 1
    Childhood-onset schizophrenia case with 2.2 Mb deletion at chromosome 3p12.2–p12.1 and two large chromosomal abnormalities at 16q22.3–q24.3 and Xq23–q28

    Childhood-onset schizophrenia case with 2.2 Mb deletion at chromosome 3p12.2–p12.1 and two large chromosomal abnormalities at 16q22.3–q24.3 and Xq23–q28 由 Rudd, Danielle, Axelsen, Michael, Epping, Eric A, Andreasen, Nancy, Wassink, Thomas

    出版 2015
    獲取全文 獲取全文 獲取全文
    Text
    加到收藏夾
    Saved in:
  2. 2
    Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism

    Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism 由 Meyer, Kacie J., Axelsen, Michael S., Sheffield, Val C., Patil, Shivanand R., Wassink, Thomas H.

    出版 2012
    獲取全文 獲取全文 獲取全文
    Text
    加到收藏夾
    Saved in:
  3. 3
    Influence of ZNF804a on Brain Structure Volumes and Symptom Severity in Individuals With Schizophrenia

    Influence of ZNF804a on Brain Structure Volumes and Symptom Severity in Individuals With Schizophrenia 由 Wassink, Thomas H., Epping, Eric A., Rudd, Danielle, Axelsen, Michael, Ziebell, Stephen, Fleming, Frank W., Monson, Eric, Choon Ho, Beng, Andreasen, Nancy C.

    出版 2012
    獲取全文 獲取全文 獲取全文
    Text
    加到收藏夾
    Saved in:

檢索工具: