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Title
Developmental and genetic perspectives on Pierre Robin sequence
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
Volume 163, Issue 4, Pages 295-305
Publisher
Wiley
Online
2013-10-14
DOI
10.1002/ajmg.c.31374
References
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Related references
Note: Only part of the references are listed.- Inactivation of LAR family phosphatase genes Ptprs and Ptprf causes craniofacial malformations resembling Pierre-Robin sequence
- (2013) K. Stewart et al. DEVELOPMENT
- Complex genomic rearrangement in theSOX95′ region in a patient with Pierre Robin sequence and hypoplastic left scapula
- (2012) Maki Fukami et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a case report and review of the literature
- (2012) Tom B Davidson et al. BMC Medical Genetics
- Educational achievements in Pierre Robin Sequence
- (2012) Martin Persson et al. Journal of Plastic Surgery and Hand Surgery
- FAF1, a Gene that Is Disrupted in Cleft Palate and Has Conserved Function in Zebrafish
- (2011) Michella Ghassibe-Sabbagh et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Toriello-Carey syndrome with a 6Mb interstitial deletion at 22q12 detected by array CGH
- (2011) Edith Said et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate
- (2011) Trilochan Sahoo et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Mandibular Distraction Osteogenesis in Infants Younger Than 3 Months
- (2011) Andrew R. Scott et al. Archives of Facial Plastic Surgery
- Prevalence of Dental Anomalies in Nonsyndromic Individuals with Cleft Lip and Palate: A Systematic Review and Meta-analysis
- (2011) Patricia Nivoloni Tannure et al. CLEFT PALATE-CRANIOFACIAL JOURNAL
- Downregulation of Dlx5 and Dlx6 expression by Hand2 is essential for initiation of tongue morphogenesis
- (2011) F. Barron et al. DEVELOPMENT
- Robin Sequence: From Diagnosis to Development of an Effective Management Plan
- (2011) K. N. Evans et al. PEDIATRICS
- The Meckel’s cartilage in human embryonic and early fetal periods
- (2010) Marzena Wyganowska-Świątkowska et al. ANATOMICAL SCIENCE INTERNATIONAL
- Clefts of the Secondary Palate Referred to the Oslo Cleft Team: Epidemiology and Cleft Severity in 994 Individuals
- (2010) Els-Marie Andersson et al. CLEFT PALATE-CRANIOFACIAL JOURNAL
- Side of Dental Anomalies and Taurodontism as Potential Clinical Markers for Cleft Subphenotypes
- (2010) Erika Calvano Küchler et al. CLEFT PALATE-CRANIOFACIAL JOURNAL
- Distraction osteogenesis of the mandible for airway obstruction in children: Long-term results
- (2010) Robert J. Tibesar et al. OTOLARYNGOLOGY-HEAD AND NECK SURGERY
- Prdm16 is required for normal palatogenesis in mice
- (2009) Bryan C. Bjork et al. HUMAN MOLECULAR GENETICS
- Clinical Experience With the Application of Distraction Osteogenesis for Airway Obstruction
- (2009) David G. Genecov et al. JOURNAL OF CRANIOFACIAL SURGERY
- Unraveling Human Cleft Lip and Palate Research
- (2009) A.R. Vieira JOURNAL OF DENTAL RESEARCH
- Long-range regulation at the SOX9 locus in development and disease
- (2009) C T Gordon et al. JOURNAL OF MEDICAL GENETICS
- Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence
- (2009) Sabina Benko et al. NATURE GENETICS
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