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A homozygous PAX3 mutation leading to severe presentation of Waardenburg syndrome with a prenatal diagnosis. [electronic resource] by
- 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, Nadège
- Chiesa, Jean
- Pingault, Véronique
Producer: 20161028
In:
Prenatal diagnosis vol. 35
Availability: No items available.
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