De Novo Alu-Element Insertions in FGFR2 Identify a Distinct Pathological Basis for Apert Syndrome
The American Journal of Human Genetics1999Vol. 64(2), pp. 446–461
Citations Over TimeTop 10% of 1999 papers
Michael Oldridge, Elaine H. Zackai, Donna M. McDonald‐McGinn, Sachiko Iseki, Gillian Morriss‐Kay, Stephen R.F. Twigg, David Johnson, Steven A. Wall, Wen G. Jiang, Christiane Theda, Ethylin Wang Jabs, Andrew O.M. Wilkie
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