Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2007.00736.x/fullpdf
Reference30 articles.
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2. A clinical and genetic study of campomelic dysplasia;Mansour;J Med Genet,1995
3. The phenotype of survivors of campomelic dysplasia;Mansour;J Med Genet,2002
4. Camptomelic dwarfism. A genetically determined mesenchymal disorder combined with sex reversal;Hovmöller;Hereditas,1977
5. Campomelic dysplasia associated with a de novo 2q;17q reciprocal translocation;Young;J Med Genet,1992
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