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Jackson-Weiss syndrome: identification of two novel FGFR2 missense mutations shared with Crouzon and Pfeiffer craniosynostotic disorders

✍ Scribed by M. Tartaglia; C. Di Rocco; Elisabeth Lajeunie; Sonia Valeri; F. Velardi; Piero A. Battaglia


Book ID
106136798
Publisher
Springer
Year
1997
Tongue
English
Weight
120 KB
Volume
101
Category
Article
ISSN
0340-6717

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