| Unbound MEDLINE results for: | Bookmark this site | | Articles related to 11039354 [Unique ID], provided by the PubMed system | |
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| | 1 - 10 of 163 journal articles in the PubMed database | Email to a friend | | |
| Robson CD, Mulliken JB, Robertson RL, et al.
Prominent basal emissary foramina in syndromic craniosynostosis: correlation with phenotypic and molecular diagnoses. [Journal Article]
AJNR Am J Neuroradiol 2000 Oct; 21(9):1707-17.
Abstract | Full Citation | Find Related Articles | | Mulliken JB, Steinberger D, Kunze S, et al.
Molecular diagnosis of bilateral coronal synostosis. [Journal Article, Review]
Plast Reconstr Surg 1999 Nov; 104(6):1603-15.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Kan SH, Elanko N, Johnson D, et al.
Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis. [Journal Article]
Am J Hum Genet 2002 Feb; 70(2):472-86.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Passos-Bueno MR, Sertié AL, Richieri-Costa A, et al.
Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses. [Journal Article]
Am J Med Genet 1998 Jul 7; 78(3):237-41.
Abstract | Full Citation | Find Related Articles | | Ito S, Sekido K, Kanno H, et al.
Phenotypic diversity in patients with craniosynostoses unrelated to Apert syndrome: the role of fibroblast growth factor receptor gene mutations. [Journal Article]
J Neurosurg 2005 Jan; 102(1 Suppl):23-30.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Preising MN, Schindler S, Friedrich M, et al.
[On the effect of mutations of the fibroblast growth factor receptors as exemplified by three cases of craniosynostoses] [Case Reports, Journal Article]
Klin Monatsbl Augenheilkd 2003 Oct; 220(10):669-81.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Tokumaru AM, Barkovich AJ, Ciricillo SF, et al.
Skull base and calvarial deformities: association with intracranial changes in craniofacial syndromes. [Journal Article]
AJNR Am J Neuroradiol 1996 Apr; 17(4):619-30.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Arnaud-López L, Fragoso R, Mantilla-Capacho J, et al.
Crouzon with acanthosis nigricans. Further delineation of the syndrome. [Journal Article]
Clin Genet 2007 Nov; 72(5):405-10.
Abstract | Full Citation | Find Related Articles | | Meyers GA, Orlow SJ, Munro IR, et al.
Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans. [Journal Article]
Nat Genet 1995 Dec; 11(4):462-4.
Abstract | Full Citation | Publisher Full Text | Find Related Articles |   |
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