• |
  • |
  • |
  • |
Donate

Product

A noevel heteroxygous deletion and insertion mutation in COL1A2 in family with overlapping features of ostergenesis imperefcta and Ehlers-Danlos syndrome.

Center:
Fiscal Year:
2011
Contact Information:
Product Description:
Keyword(s):
Product/Publication Type(s):
Conference presentations and posters presented
Target Audience:
Professionals
Alternative Format:
To Obtain Copies (URL or Email):
na
COVID-19 Related Data:
N/A