A prenatal case of partial trisomy 21 (q22.2q22.3),...

A prenatal case of partial trisomy 21 (q22.2q22.3), resulting from a paternal insertion translocation ins(16;21) and uncovered by QF-PCR, and characterized by array CGH and FISH

Bhola, Shama L., Nieuwint, Aggie W. M., Stuurman, Kyra E.
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:
6
Language:
english
Journal:
Clinical Case Reports
DOI:
10.1002/ccr3.1563
Date:
July, 2018
File:
PDF, 940 KB
english, 2018
Conversion to is in progress
Conversion to is failed