A homozygous PAX3 mutation...

Prenatal Diagnosis 2015 / 12 Vol. 35; Iss. 13

A homozygous PAX3 mutation leading to severe presentation of Waardenburg syndrome with a prenatal diagnosis

Mousty, Eve, Issa, Sarah, Grosjean, Frédéric, Col, Jean-Yves, Khau Van Kien, Philippe, Perez, Marie-Josée, Petrov, Yuliya, Reboul, Dorothée, Faubert, Emmanuelle, Le Gac, Marie-Pascale, Bondurand, Nadè
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:
35
Language:
english
Journal:
Prenatal Diagnosis
DOI:
10.1002/pd.4703
Date:
December, 2015
File:
PDF, 117 KB
english, 2015
Conversion to is in progress
Conversion to is failed