U.S. flag

An official website of the United States government

Display Settings:

Format
Sort by

Send to:

Choose Destination

Links from Nucleotide

Items: 3

1.
Erratum
Linglart et al. (May 2005 76:804–814)
Am J Hum Genet. 2007 Jul; 81(1): 196.
Corrects:
Am J Hum Genet. 2005 May; 76(5): 804–814.
PMCID:
PMC1950928
CorrectionPDF–127K
2.
A Novel STX16 Deletion in Autosomal Dominant Pseudohypoparathyroidism Type Ib Redefines the Boundaries of a cis-Acting Imprinting Control Element of GNAS
Agnès Linglart, Robert C. Gensure, Robert C. Olney, Harald Jüppner, Murat Bastepe
Am J Hum Genet. 2005 May; 76(5): 804–814. Published online 2005 Mar 30. doi: 10.1086/429932
Correction in:
Am J Hum Genet. 2007 Jul; 81(1): 196.
PMCID:
PMC1199370
AbstractArticlePDF–541K
3.
Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS
Murat Bastepe, Leopold F. Fröhlich, Geoffrey N. Hendy, Olafur S. Indridason, Robert G. Josse, Hiroyuki Koshiyama, Jarmo Körkkö, Jon M. Nakamoto, Arlan L. Rosenbloom, Arnold H. Slyper, Toshitsugu Sugimoto, Agathocles Tsatsoulis, John D. Crawford, Harald Jüppner
J Clin Invest. 2003 Oct 15; 112(8): 1255–1263. doi: 10.1172/JCI19159
PMCID:
PMC213493
AbstractArticlePDF–875K

Display Settings:

Format
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI > Literature > PubMed Central (PMC)
Support Center