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- [1] Mutations in TFAP2B and previously unimplicated genes of the BMP, Wnt, and Hedgehog pathways in syndromic craniosynostosisPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 116 (30) : 15116 - 15121Timberlake, Andrew T.Jin, Sheng ChihNelson-Williams, CarolWu, RobinFurey, Charuta G.Islam, BariraHaider, ShozebLoring, ErinGalm, AmySteinbacher, Derek M.Larysz, DawidStaffenberg, David A.Flores, Roberto L.Rodriguez, Eduardo D.Boggon, Titus J.Persing, John A.Lifton, Richard P.
- [2] Mutations in TFAP2B and previously unimplicated genes of the BMP, Wnt, and Hedgehog pathways in syndromic craniosynostosis (vol 116, pg 15116, 2019)PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 116 (34) : 17130 - 17130Timberlake, Andrew T.Jin, Sheng ChihNelson-Williams, CarolWu, RobinFurey, Charuta G.Islam, BariraHaider, ShozebLoring, ErinGalm, Amy
- [3] Syndromic patent ductus arteriosus:: Evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorderPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (08) : 2975 - 2979Mani, ARadhakrishnan, JFarhi, ACarew, KSWarnes, CANelson-Williams, CDay, RWPober, BState, MWLifton, RP
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- [5] De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosisJOURNAL OF NEUROSURGERY, 2018, 128 (04) : 83 - 83Furey, Charuta G.Timberlake, AndrewNelson-Williams, CarolDiLuna, MichaelKahle, KristopherSteinbacher, DerekLarysz, DawidPersing, JohnLifton, Richard
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- [7] Familial Nonsyndromic Patent Ductus Arteriosus Caused by Mutations in TFAP2BPediatric Cardiology, 2011, 32 : 958 - 965Yi-Wei ChenWu ZhaoZhi-Fang ZhangQihua FuJie ShenZhen ZhangWei JiJian WangFen Li
- [8] Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosusNATURE GENETICS, 2000, 25 (01) : 42 - 46Satoda, MZhao, FDiaz, GABurn, JGoodship, JDavidson, HRPierpont, MEMGelb, BD
- [9] Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosusNature Genetics, 2000, 25 : 42 - 46Masahiko SatodaFeng ZhaoGeorge A. DiazJohn BurnJudith GoodshipH. Rosemarie DavidsonMary Ella M. PierpontBruce D. Gelb
- [10] Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlationAMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 695 - 703Zhao, FWeismann, CGSatoda, MPierpont, MEMSweeney, EThompson, EMGelb, BD