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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

74 related items for PubMed ID: 21233754

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  • 7. [A case of bilateral coronal craniosynostosis with the P250R mutation in FGFR3 gene].
    Mori F, Kuwajima K, Yamanaka K, Kondou I.
    No To Hattatsu; 2001 Jan; 33(1):53-7. PubMed ID: 11197897
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  • 9. Molecular analysis of patients with synostotic frontal plagiocephaly (unilateral coronal synostosis).
    Mulliken JB, Gripp KW, Stolle CA, Steinberger D, Müller U.
    Plast Reconstr Surg; 2004 Jun; 113(7):1899-909. PubMed ID: 15253176
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  • 13. EFNB1 mutation at the ephrin ligand-receptor dimerization interface in a patient with craniofrontonasal syndrome.
    Torii C, Izumi K, Nakajima H, Takahashi T, Kosaki K.
    Congenit Anom (Kyoto); 2007 Mar; 47(1):49-52. PubMed ID: 17300690
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  • 14. Muenke syndrome: Medical and surgical comorbidities and long-term management.
    Murali CN, McDonald-McGinn DM, Wenger TL, McDougall C, Stroup BM, Sheppard SE, Taylor J, Bartlett SP, Bhoj EJ, Zackai EH, Santani A.
    Am J Med Genet A; 2019 Aug; 179(8):1442-1450. PubMed ID: 31111620
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  • 16. Syndrome of coronal craniosynostosis, Klippel-Feil anomaly, and sprengel shoulder with and without Pro250Arg mutation in the FGFR3 gene.
    Lowry RB, Jabs EW, Graham GE, Gerritsen J, Fleming J.
    Am J Med Genet; 2001 Nov 22; 104(2):112-9. PubMed ID: 11746040
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  • 17. Muenke syndrome: An international multicenter natural history study.
    Kruszka P, Addissie YA, Yarnell CM, Hadley DW, Guillen Sacoto MJ, Platte P, Paelecke Y, Collmann H, Snow N, Schweitzer T, Boyadjiev SA, Aravidis C, Hall SE, Mulliken JB, Roscioli T, Muenke M.
    Am J Med Genet A; 2016 Apr 22; 170A(4):918-29. PubMed ID: 26740388
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