A 785 kb deletion of 3p14.1p13, including the...

European Journal of Medical Genetics 2009 Vol. 52; Iss. 2-3

A 785 kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis

Mitchel J. Pariani, Andrew Spencer, John M. Graham Jr., David L. Rimoin
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
52
Year:
2009
Language:
english
Pages:
128
DOI:
10.1016/j.ejmg.2009.03.012
File:
PDF, 429 KB
english, 2009
Conversion to is in progress
Conversion to is failed