Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

27 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Familial short stature is associated with a novel dominant-negative heterozygous insulin-like growth factor 1 receptor (IGF1R) mutation.
Kawashima Y, Hakuno F, Okada S, Hotsubo T, Kinoshita T, Fujimoto M, Nishimura R, Fukushima T, Hanaki K, Takahashi S, Kanzaki S. Kawashima Y, et al. Among authors: hotsubo t. Clin Endocrinol (Oxf). 2014 Aug;81(2):312-4. doi: 10.1111/cen.12317. Epub 2013 Sep 30. Clin Endocrinol (Oxf). 2014. PMID: 24033502 No abstract available.
The prevalence of mitochondrial gene mutations in childhood diabetes in Japan.
Matsuura N, Suzuki S, Yokota Y, Kazahari K, Kazahari M, Toyota T, Hirai M, Okuno A, Harada S, Fukushima N, Koike A, Ito Y, Hotsubo T. Matsuura N, et al. Among authors: hotsubo t. J Pediatr Endocrinol Metab. 1999 Jan-Feb;12(1):27-30. doi: 10.1515/jpem.1999.12.1.27. J Pediatr Endocrinol Metab. 1999. PMID: 10392345
27 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page