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Items: 1 to 20 of 27

1.

An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly.

Kress W, Petersen B, Collmann H, Grimm T.

Cytogenet Cell Genet. 2000;91(1-4):138-40.

PMID:
11173846
2.

Craniosynostosis: genes and mechanisms.

Wilkie AO.

Hum Mol Genet. 1997;6(10):1647-56. Review.

PMID:
9300656
3.

Craniosynostosis and related limb anomalies.

Wilkie AO, Oldridge M, Tang Z, Maxson RE Jr.

Novartis Found Symp. 2001;232:122-33; discussion 133-43. Review.

PMID:
11277076
4.
5.

Craniosynostosis syndromes: from genes to premature fusion of skull bones.

Hehr U, Muenke M.

Mol Genet Metab. 1999 Oct;68(2):139-51. Review. No abstract available.

PMID:
10527665
6.

Syndromic craniosynostosis: from history to hydrogen bonds.

Cunningham ML, Seto ML, Ratisoontorn C, Heike CL, Hing AV.

Orthod Craniofac Res. 2007 May;10(2):67-81. Review.

PMID:
17552943
7.

[From gene to disease; craniosynostosis syndromes due to FGFR2-mutation].

van Ravenswaaij-Arts CM, van den Ouweland AM, Hoogeboom AJ, Herbergs J, Pals G.

Ned Tijdschr Geneeskd. 2002 Jan 12;146(2):63-6. Review. Dutch.

PMID:
11820058
8.

Genetic basis of single-suture synostoses: genes, chromosomes and clinical implications.

Lattanzi W, Bukvic N, Barba M, Tamburrini G, Bernardini C, Michetti F, Di Rocco C.

Childs Nerv Syst. 2012 Sep;28(9):1301-10. doi: 10.1007/s00381-012-1781-1. Epub 2012 Aug 8. Review.

PMID:
22872241
9.

Roles of FGFR2 and twist in human craniosynostosis: insights from genetic mutations in cranial osteoblasts.

Marie PJ, Kaabeche K, Guenou H.

Front Oral Biol. 2008;12:144-59. doi: 10.1159/0000115036. Review.

PMID:
18391499
10.

Molecular genetics of craniosynostotic syndromes.

Müller U, Steinberger D, Kunze S.

Graefes Arch Clin Exp Ophthalmol. 1997 Sep;235(9):545-50. Review.

PMID:
9342602
11.

Craniosynostosis syndromes in the genomic era.

Aleck K.

Semin Pediatr Neurol. 2004 Dec;11(4):256-61. Review.

PMID:
15828709
12.

Cranial suture biology.

Lenton KA, Nacamuli RP, Wan DC, Helms JA, Longaker MT.

Curr Top Dev Biol. 2005;66:287-328. Review. No abstract available.

PMID:
15797457
13.

Molecular and cellular bases of syndromic craniosynostoses.

Bonaventure J, El Ghouzzi V.

Expert Rev Mol Med. 2003 Jan 29;5(4):1-17. Review.

PMID:
14987407
14.

Craniosynostosis: from a clinical description to an understanding of bone formation of the skull.

Lajeunie E, Catala M, Renier D.

Childs Nerv Syst. 1999 Nov;15(11-12):676-80. Review.

PMID:
10603009
15.

Genetics of craniosynostosis: review of the literature.

Ciurea AV, Toader C.

J Med Life. 2009 Jan-Mar;2(1):5-17. Review.

16.

Insights into the development of molecular therapies for craniosynostosis.

Kosty J, Vogel TW.

Neurosurg Focus. 2015 May;38(5):E2. doi: 10.3171/2015.2.FOCUS155. Review.

PMID:
25929964
17.

Unclassifiable craniosynostosis phenotypes, FGFR2 Trp290 mutations, acanthosis nigricans, and unpaired cysteine mutations.

Cohen MM Jr.

Am J Med Genet. 2002 Nov 15;113(1):1-3. Review. No abstract available.

PMID:
12400057
18.

Fibroblast growth factor receptor-2 mutations in craniosynostosis.

Malcolm S, Reardon W.

Ann N Y Acad Sci. 1996 Jun 8;785:164-70. Review. No abstract available.

PMID:
8702123
19.

[Antley-Bixler syndrome].

Satokata I.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):133-5. Review. Japanese. No abstract available.

PMID:
11057168
20.

Molecular diagnosis of bilateral coronal synostosis.

Mulliken JB, Steinberger D, Kunze S, Müller U.

Plast Reconstr Surg. 1999 Nov;104(6):1603-15. Review.

PMID:
10541159

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