Old Web
English
Sign In
Acemap
>
authorDetail
>
Misa Honda
Misa Honda
Tokyo Dental College
Biology
Genetics
Hypotonia
Rett syndrome
Corpus callosum
2
Papers
12
Citations
0.00
KQI
Citation Trend
Filter By
Interval:
1900~2024
1900
2024
Author
Papers (2)
Sort By
Default
Most Recent
Most Early
Most Citation
No data
Journal
Conference
Others
A novel SOX10 variant in a Japanese girl with Waardenburg syndrome type 4C and Kallmann syndrome
2020
Human genome variation
Junpei Hamada
Fumihiro Ochi
Yuka Sei
Koji Takemoto
Hiroki Hirai
Misa Honda
Hironori Shibata
Tomonobu Hasegawa
Mariko Eguchi
Show All
Source
Cite
Save
Citations (1)
A 2.0 Mb microdeletion in proximal chromosome 14q12, involving regulatory elements of FOXG1, with the coding region of FOXG1 being unaffected, results in severe developmental delay, microcephaly, and hypoplasia of the corpus callosum
2013
European Journal of Medical Genetics
Masaki Takagi
Goro Sasaki
Toshikatsu Mitsui
Misa Honda
Yoko Tanaka
Tomonobu Hasegawa
Show All
Source
Cite
Save
Citations (11)
1
map