Genetic basis of single-suture synostoses: genes, chromosomes and clinical implications
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Genetic basis of single-suture synostoses: genes, chromosomes and clinical implications
Authors
Keywords
-
Journal
CHILDS NERVOUS SYSTEM
Volume 28, Issue 9, Pages 1301-1310
Publisher
Springer Nature
Online
2012-08-07
DOI
10.1007/s00381-012-1781-1
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Evaluation and management of nonsyndromic craniosynostosis
- (2011) F Ursitti et al. ACTA PAEDIATRICA
- Craniosynostosis
- (2011) David Johnson et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Cleft lip and palate: understanding genetic and environmental influences
- (2011) Michael J. Dixon et al. NATURE REVIEWS GENETICS
- IGF1R variants associated with isolated single suture craniosynostosis
- (2010) Michael L. Cunningham et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Copy number variation analysis in single-suture craniosynostosis: Multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis
- (2010) Heather C. Mefford et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Familial X;Y translocation with distinct phenotypic consequences: Characterization using FISH and array CGH
- (2010) N. Bukvic et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Letters to the Editor
- (2010) CARSTEN PEDERSEN CLINICAL GENETICS
- Autosomal dominant craniosynostosis of the sutura metopica
- (2010) Raoul C. M. Hennekam et al. CLINICAL GENETICS
- CCMG guidelines: prenatal and postnatal diagnostic testing for uniparental disomy
- (2010) AJ Dawson et al. CLINICAL GENETICS
- Signaling networks in RUNX2-dependent bone development
- (2010) Toshihisa Komori JOURNAL OF CELLULAR BIOCHEMISTRY
- Long-term neuropsychological development in single-suture craniosynostosis treated early
- (2010) Daniela Chieffo et al. Journal of Neurosurgery-Pediatrics
- Prevalence and Complications of Single-Gene and Chromosomal Disorders in Craniosynostosis
- (2010) A. O. M. Wilkie et al. PEDIATRICS
- Perspectives onRUNXgenes: An update
- (2009) M. Michael Cohen Jr. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- The Increase of Metopic Synostosis
- (2009) Jacques van der Meulen et al. JOURNAL OF CRANIOFACIAL SURGERY
- Evolution in the frequency of nonsyndromic craniosynostosis
- (2009) Federico Di Rocco et al. Journal of Neurosurgery-Pediatrics
- Autism and Hypoplastic Corpus Callosum in a Case of Monocentric Marker Chromosome 15
- (2009) Jadranka D. Jovanović-Privrodski et al. PEDIATRIC NEUROLOGY
- The Changing Epidemiologic Spectrum of Single-Suture Synostoses
- (2009) Jesse Selber et al. PLASTIC AND RECONSTRUCTIVE SURGERY
- Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype
- (2008) Mariëlle E.M. Swinkels et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Familial Lambdoid Craniosynostosis Between Father and Son
- (2008) Natacha Kadlub et al. JOURNAL OF CRANIOFACIAL SURGERY
- TWIST microdeletion identified by array CGH in a patient presenting Saethre–Chotzen phenotype and a complex rearrangement involving chromosomes 2 and 7
- (2007) Caroline Schluth-Bolard et al. European Journal of Medical Genetics
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now