Rare mutations of FGFR2 causing Apert syndrome %25253A ident…
Rare mutations of FGFR2 causing Apert syndrome %25253A identification of the first partial gene deletion%25252C and an Alu element insertion from a new subfamily
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Journal:
Human MutationOpens in new Window
Coverage:
- 1996~present; volume:7~present;issue:1~present
Journal:
Human MutationOpens in new Window
Coverage:
- 1996-01-01~present; volume:7~present;issue:1~present