DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Al-Haggar M, Yahia S, Damjanovich K, Ahmad N, Hamada I, Bayrak-Toydemir P.
p.R672C mutation of MYH3 gene in an Egyptian infant presented with Freeman-Sheldon syndrome.
Indian J Pediatr 2011;
78 (01) 103-105
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