Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Chi-Fung Jennifer Chen"'
Autor:
Chi-Fung Jennifer Chen, Angela Jiang, Heileen Hsu-Kim, Katherine Xu, Jessica A. Shuen, Allison R. Elia, Aubrey Bonhivert, Ellen Litkowski, Rochelle D. Schwartz-Bloom
Publikováno v:
Journal of Women and Minorities in Science and Engineering. 17:295-312
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf59d7ecde04b5ba72495ed324b01d8d
https://doi.org/10.1615/jwomenminorscieneng.2011002292
https://doi.org/10.1615/jwomenminorscieneng.2011002292
Autor:
Ellen Litkowski, Allison R. Elia, Jessica A. Shuen, Rochelle D. Schwartz-Bloom, Aubrey Bonhivert, Angela Jiang, Heileen Hsu-Kim, Katherine Xu, Chi-Fung Jennifer Chen
Publikováno v:
Journal of Women and Minorities in Science and Engineering. 17:313-324
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32d80edbc6ff2ce424370f96ecf75c83
https://doi.org/10.1615/jwomenminorscieneng.2011002293
https://doi.org/10.1615/jwomenminorscieneng.2011002293
Autor:
Ken-Shiung Chen, Tew Wai Loon, Low Hai Loon, Hew Choy Sin, Chi-Chen Kevin Chen, Chi-Fung Jennifer Chen
Publikováno v:
Advanced Topics in Neurological Disorders
Angelman syndrome (AS) is a genetic disorder with an incidence of 1 in 15,000, and it was first described in 1965 by Harry Angelman (1,2). It is characterized by a severe developmental delay together with mental disorders, movement disorders and beha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acb67fcad8080f3557cf7aa6a1819d80
http://www.intechopen.com/articles/show/title/angelman-syndrome-proteomics-analysis-of-an-ube3a-knockout-mouse-and-its-implications
http://www.intechopen.com/articles/show/title/angelman-syndrome-proteomics-analysis-of-an-ube3a-knockout-mouse-and-its-implications
Autor:
Yen-Juin Chen, Chi-Fung Jennifer Chen, Chi-Yu Huang, Shuan-Pei Lin, Aihua Hou, Chih-Kuang Chuang, Ken-Shiung Chen, Hsiang-Yu Lin, Shi Yun Ho, Huei-Ching Chiu
Publikováno v:
Annals of Human Genetics.
Summary Prader–Willi syndrome (PWS) is a neurogenetic disorder associated with recurrent genomic recombination involving low copy repeats (LCRs) located in the human chromosome 15q11-q13. Previous studies of PWS patients from Asia suggested that th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0027f1d5f2b56d42e55b7065fe35984a
https://doi.org/10.1111/j.1469-1809.2010.00633.x
https://doi.org/10.1111/j.1469-1809.2010.00633.x
Publikováno v:
Neurourology & Urodynamics; Oct2007, Vol. 26 Issue 6, p820-827, 8p