Analysis of variation in expression of autosomal dominant osteopetrosis type 2: Searching for modifier genes
- 30 November 2005
- Vol. 37 (5) , 655-661
- https://doi.org/10.1016/j.bone.2005.06.003
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Cathepsin L‐deficient mice exhibit abnormal skin and bone development and show increased resistance to osteoporosis following ovariectomyInternational Journal of Experimental Pathology, 2004
- Chloride Channel ClCN7 Mutations Are Responsible for Severe Recessive, Dominant, and Intermediate OsteopetrosisJournal of Bone and Mineral Research, 2003
- Chloride Channel 7 (ClCN7) Gene Mutations and Autosomal Dominant Osteopetrosis, Type IIJournal of Bone and Mineral Research, 2003
- Measurement of Tartrate-Resistant Acid Phosphatase and the Brain Isoenzyme of Creatine Kinase Accurately Diagnoses Type II Autosomal Dominant Osteopetrosis but Does Not Identify Gene CarriersJournal of Clinical Endocrinology & Metabolism, 2002
- Albers-Schonberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel geneHuman Molecular Genetics, 2001
- Immunohistochemical detection of parathyroid hormone-related peptide, Indian hedgehog, and patched in the process of endochondral ossification in the humanHistochemistry and Cell Biology, 2001
- Modifier genes in mice and humansNature Reviews Genetics, 2001
- The Power to Detect Linkage in Complex Disease by Means of Simple LOD-Score AnalysesAmerican Journal of Human Genetics, 1998
- PedCheck: A Program for Identification of Genotype Incompatibilities in Linkage AnalysisAmerican Journal of Human Genetics, 1998
- OSTEOPETROSISMedicine, 1968