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Results: 10

1.

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome.

Reardon W, Winter RM, Rutland P, Pulleyn LJ, Jones BM, Malcolm S.

Nat Genet. 1994 Sep;8(1):98-103.

PMID:
7987400
[PubMed - indexed for MEDLINE]
2.

Apert and Crouzon syndromes: clinical findings, genes and extracellular matrix.

Carinci F, Pezzetti F, Locci P, Becchetti E, Carls F, Avantaggiato A, Becchetti A, Carinci P, Baroni T, Bodo M.

J Craniofac Surg. 2005 May;16(3):361-8. Review.

PMID:
15915098
[PubMed - indexed for MEDLINE]
3.

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
[PubMed - indexed for MEDLINE]
4.

[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
[PubMed - indexed for MEDLINE]
5.

Pfeiffer syndrome type 2: further delineation and review of the literature.

Plomp AS, Hamel BC, Cobben JM, Verloes A, Offermans JP, Lajeunie E, Fryns JP, de Die-Smulders CE.

Am J Med Genet. 1998 Jan 23;75(3):245-51. Review.

PMID:
9475590
[PubMed - indexed for MEDLINE]
6.

[Molecular genetics of congenital skeletal dysplasias related to mutations of fibroblast growth factor receptors].

Sanak M.

Med Wieku Rozwoj. 1999 Jan-Mar;3(1):67-82. Review. Polish.

PMID:
10910640
[PubMed - indexed for MEDLINE]
7.

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
[PubMed - indexed for MEDLINE]
8.

[Crouzon syndrome].

Murano I.

Nihon Rinsho. 2006 Sep 28;Suppl 3:416-7. Review. Japanese. No abstract available.

PMID:
17022577
[PubMed - indexed for MEDLINE]
9.

[Presentation of two cases of Crouzon syndrome: allelic cranio-stenotic conditions of FGFR genes].

Vidal Sanahuja R, Gean Molins E, Sánchez Garré C, Quilis Esquerra J, García Fructuoso G, Costa Clara JM.

An Pediatr (Barc). 2012 Oct;77(4):272-8. doi: 10.1016/j.anpedi.2012.03.024. Epub 2012 May 26. Review. Spanish.

PMID:
22633821
[PubMed - indexed for MEDLINE]
Free Article
10.

[Molecular mechanisms of carcinogenesis in human stomach cancer: K-sam gene].

Yoshida K, Toge T, Kuniyasu H, Yasui W, Tahara E.

Nihon Rinsho. 2001 Apr;59 Suppl 4:53-9. Review. Japanese. No abstract available.

PMID:
11424439
[PubMed - indexed for MEDLINE]

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