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Rare mutations of FGFR2 causing Apert syndrome %3A identific…

Rare mutations of FGFR2 causing Apert syndrome %3A identification of the first partial gene deletion%2C and an Alu element insertion from a new subfamily

Article, Chapter

Authors: E.G. Bochukova

Publication: Human Mutation, Volume:30, Issue:2, Page(s):-211

Published: Wiley, 2009

ISSN: 1059-7794

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View Full Text Source:Human Mutation,Human Mutation,Wiley Online Library Database Model 2021 Opens in new Window

Journal: Human Mutation Source:Wiley Online Library Database Model 2021 Opens in new Window

Collection: Wiley Online Library Database Model 2021 Opens in new Window

Coverage:

1996~present; volume:7~present;issue:1~present

View Full Text Source:Human Mutation,Human Mutation,Wiley Online Library: Complete Journals Opens in new Window

Journal: Human Mutation Source:Wiley Online Library: Complete Journals Opens in new Window

Collection: Wiley Online Library: Complete Journals Opens in new Window

Coverage:

1996-01-01~present; volume:7~present;issue:1~present

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