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Diverse clinical and genetic aspects of craniofrontonasal syndrome.
Zafeiriou DI, Pavlidou EL, Vargìami E. Zafeiriou DI, et al. Pediatr Neurol. 2011 Feb;44(2):83-7. doi: 10.1016/j.pediatrneurol.2010.10.012. Pediatr Neurol. 2011. PMID: 21215906 Review.
Craniofrontonasal syndrome is characterized by coronal craniosynostosis, hypertelorism, telecanthus, a broad grooved nasal tip, dental anomalies, mild syndactyly, and broad thumbs. ...
Craniofrontonasal syndrome is characterized by coronal craniosynostosis, hypertelorism, telecanthus, a broad grooved nasal tip
Clinical and genetic aspects of craniofrontonasal syndrome: towards resolving a genetic paradox.
Wieacker P, Wieland I. Wieacker P, et al. Mol Genet Metab. 2005 Sep-Oct;86(1-2):110-6. doi: 10.1016/j.ymgme.2005.07.017. Mol Genet Metab. 2005. PMID: 16143553 Review.
Craniofrontonasal syndrome (CFNS) is characterized by body asymmetry, midline defects, skeletal abnormalities, and dermatological abnormalities. ...
Craniofrontonasal syndrome (CFNS) is characterized by body asymmetry, midline defects, skeletal abnormalities, and dermatologi
Clinical features of syndromic craniosynostosis.
Rice DP. Rice DP. Front Oral Biol. 2008;12:91-106. doi: 10.1159/000115034. Front Oral Biol. 2008. PMID: 18391497 Review.
More than 100 syndromes in which craniosynostosis is a feature have been documented and here the most common conditions including Apert and Crouzon syndromes are described as well as other conditions with a particularly interesting molecular etiology, such as Saethre- Chotzen and …
More than 100 syndromes in which craniosynostosis is a feature have been documented and here the most common conditions including Apert and …
Bone cell interactions through Eph/ephrin: bone modeling, remodeling and associated diseases.
Matsuo K, Otaki N. Matsuo K, et al. Cell Adh Migr. 2012 Mar-Apr;6(2):148-56. doi: 10.4161/cam.20888. Epub 2012 Mar 1. Cell Adh Migr. 2012. PMID: 22660185 Free PMC article. Review.
Migration, attachment and spreading of mesenchymal stem cells are regulated by ephrinB ligands and EphB receptors. ephrinB1 loss-of-function is associated with craniofrontonasal syndrome (CFNS) in humans and mice. In bone remodeling, ephrinB2 is postulated to act as …
Migration, attachment and spreading of mesenchymal stem cells are regulated by ephrinB ligands and EphB receptors. ephrinB1 loss-of-function …
Craniofrontonasal dysplasia: phenotypic expression in females and males and genetic considerations.
Grutzner E, Gorlin RJ. Grutzner E, et al. Oral Surg Oral Med Oral Pathol. 1988 Apr;65(4):436-44. doi: 10.1016/0030-4220(88)90358-1. Oral Surg Oral Med Oral Pathol. 1988. PMID: 3283635 Review.
The phenotype and pattern of inheritance of craniofrontonasal dysplasia were analyzed in 66 affected persons from 18 families, including one four-generation kindred personally studied. ...
The phenotype and pattern of inheritance of craniofrontonasal dysplasia were analyzed in 66 affected persons from 18 families, …
Craniofrontonasal dysostosis with deafness and axillary pterygia.
Michels VV, Derleth DP, Hoffman AD, Goldston AS. Michels VV, et al. Am J Med Genet. 1989 Nov;34(3):445-50. doi: 10.1002/ajmg.1320340323. Am J Med Genet. 1989. PMID: 2688423 Review.
Craniofrontonasal dysostosis (CFND) is an inherited disorder previously referred to as craniofrontonasal dysplasia. However, there is no evidence of tissue dysplasia and, therefore, the term dysostosis has been substituted. ...
Craniofrontonasal dysostosis (CFND) is an inherited disorder previously referred to as craniofrontonasal dysplasia. However, t …
Craniofrontonasal dysplasia.
Schaefer GB, Olney AH, Kolodziej P. Schaefer GB, et al. Ear Nose Throat J. 1998 Feb;77(2):90. Ear Nose Throat J. 1998. PMID: 9509720 Review. No abstract available.
[Craniofrontonasal dysplasia].
Kurosawa K. Kurosawa K. Ryoikibetsu Shokogun Shirizu. 2001;(33):513-4. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462544 Review. Japanese. No abstract available.