Localization of Familial Benign Hypercalcemia, Oklahoma Variant (FBHOk), to Chromosome 19q13
- 1 January 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (1) , 189-195
- https://doi.org/10.1086/302202
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Identification of Putative Transmembrane Receptor Sequences Homologous to the Calcium-Sensing G-Protein-Coupled ReceptorGenomics, 1997
- Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1)Human Genetics, 1997
- Calcium‐sensing receptor mutations in familial hypocalciuric hypercalcaemia with recurrent pancreatitisClinical Endocrinology, 1996
- A common molecular basis for three inherited kidney stone diseasesNature, 1996
- Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism.Journal of Clinical Investigation, 1995
- An integrated metric physical map of human chromosome 19Nature Genetics, 1995
- Genetic Linkage Mapping of the Dehydroepiandrosterone Sulfotransferase (STD) Gene on the Chromosome 19q13.3 RegionGenomics, 1995
- Minireview: Mutations and Diseases of G Protein Coupled ReceptorsJournal of Receptors and Signal Transduction, 1995
- Structure of the Human CALM1 Calmodulin Gene and Identification of two CALM1 ‐Related Pseudogenes CALM1P1 and CALM1P2European Journal of Biochemistry, 1994
- The 1993–94 Généthon human genetic linkage mapNature Genetics, 1994