In vitro studies on clonal growth of chondrocytes in thanatophoric dysplasia
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference21 articles.
1. A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
2. Lethal neonatal chondrodysplasias in the west of scotland 1970-1983 with a description of a thanatophoric, dysplasialike, autosomal recessive disorder, glasgow variant
3. Type II collagen screening in the human chondrodysplasias
4. Receptors for the TGF-β family
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1. The paradox of FGFR3 signaling in skeletal dysplasia: Why chondrocytes growth arrest while other cells over proliferate;Mutation Research/Reviews in Mutation Research;2014-01
2. From Genotype to Phenotype: The Differential Expression of FGF, FGFR, and TGFβ Genes Characterizes Human Cranioskeletal Development and Reflects Clinical Presentation in FGFR Syndromes;Plastic and Reconstructive Surgery;2001-12
3. Enanismo tanatofórico en embarazo gemelar;Anales de Pediatría;2000
4. Structural roles of acetylcholinesterase variants in biology and pathology;European Journal of Biochemistry;1999-09-15
5. Human Osteogenesis Involves Differentiation-Dependent Increases in the Morphogenically Active 3′ Alternative Splicing Variant of Acetylcholinesterase;Molecular and Cellular Biology;1999-01
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