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A novel de novo heterozygous mutation in FGFR1 is associated with Hartsfield syndrome
A novel de novo heterozygous mutation in FGFR1 is associated with Hartsfield syndrome
2014
Rathi Prasad
Carole Brewer
Christine Burren
Keywords:
Genetics
Hartsfield Syndrome
Fibroblast growth factor receptor 1
Mutation
Medicine
Biology
heterozygous mutation
Correction
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