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Germline mutation in BRAF codon 600 is compatible with human development: de novo p.V600G mutation identified in a patient with CFC syndrome

✍ Scribed by KJ Champion; C Bunag; AL Estep; JR Jones; CH Bolt; RC Rogers; KA Rauen; DB Everman


Book ID
110889099
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
913 KB
Volume
79
Category
Article
ISSN
0009-9163

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