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Assignment ofFGF8to Human Chromosome 10q25–q26: Mutations inFGF8May Be Responsible for Some Types of Acrocephalosyndactyly Linked to This Region

✍ Scribed by ROBERT A. WHITE; LISA L. DOWLER; STEVEN V. ANGELONI; LINDA M. PASZTOR; CRAIG A. MACARTHUR


Book ID
115612549
Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
69 KB
Volume
30
Category
Article
ISSN
0888-7543

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