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Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype

✍ Scribed by G D'Amours; Z Kibar; G Mathonnet; R Fetni; F Tihy; V Désilets; S Nizard; JL Michaud; E Lemyre


Book ID
110889267
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
751 KB
Volume
81
Category
Article
ISSN
0009-9163

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