A common FGFR3 gene mutation is present in achondroplasia but not in hypochondroplasia
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference27 articles.
1. Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4
2. Fibroblast growth factor receptor (FGFR) 3. Alternative splicing in immunoglobulin-like domain III creates a receptor highly specific for acidic FGF/FGF-1
3. Localization of the achondroplasia gene to the distal 2. 5 Mb of human chromosome 4p
4. Germinal mosaicism in achondroplasia: a family with 3 affected siblings of normal parents
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