Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1999 | 1 |
2000 | 1 |
2001 | 1 |
2005 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 1386327
4 results
Results by year
Filters applied: . Clear all
Page 1
Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism.
J Med Genet. 2005 May;42(5):443-8. doi: 10.1136/jmg.2004.026898.
J Med Genet. 2005.
PMID: 15863676
Free PMC article.
No abstract available.
Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB.
Ding C, Buckingham B, Levine MA.
Ding C, et al.
J Clin Invest. 2001 Oct;108(8):1215-20. doi: 10.1172/JCI13180.
J Clin Invest. 2001.
PMID: 11602629
Free PMC article.
Item in Clipboard
Genetic ablation of parathyroid glands reveals another source of parathyroid hormone.
Günther T, Chen ZF, Kim J, Priemel M, Rueger JM, Amling M, Moseley JM, Martin TJ, Anderson DJ, Karsenty G.
Günther T, et al.
Nature. 2000 Jul 13;406(6792):199-203. doi: 10.1038/35018111.
Nature. 2000.
PMID: 10910362
Item in Clipboard
Isolation and expression analysis of a novel human homologue of the Drosophila glial cells missing (gcm) gene.
Kanemura Y, Hiraga S, Arita N, Ohnishi T, Izumoto S, Mori K, Matsumura H, Yamasaki M, Fushiki S, Yoshimine T.
Kanemura Y, et al.
FEBS Lett. 1999 Jan 15;442(2-3):151-6. doi: 10.1016/s0014-5793(98)01650-0.
FEBS Lett. 1999.
PMID: 9928992
Free article.
Item in Clipboard
Cite
Cite