A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes

Mohammad K. Hajihosseini, Stephen Wilson, Laurence De Moerlooze, Clive Dickson

Research output: Contribution to journal › Article › peer-review

143 Citations (Scopus)

Original language	English
Pages (from-to)	3855-3860
Number of pages	6
Journal	Proceedings of the National Academy of Sciences
Volume	98
Issue number	7
DOIs	https://doi.org/10.1073/pnas.071586898
Publication status	Published - 2001

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title = "A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes",

author = "Hajihosseini, {Mohammad K.} and Stephen Wilson and {De Moerlooze}, Laurence and Clive Dickson",

year = "2001",

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T1 - A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes

AU - Hajihosseini, Mohammad K.

AU - Wilson, Stephen

AU - De Moerlooze, Laurence

AU - Dickson, Clive

PY - 2001

Y1 - 2001

U2 - 10.1073/pnas.071586898

DO - 10.1073/pnas.071586898

M3 - Article

VL - 98

SP - 3855

EP - 3860

JO - Proceedings of the National Academy of Sciences of the United States of America

JF - Proceedings of the National Academy of Sciences of the United States of America

SN - 0027-8424

IS - 7

ER -