Related references
Note: Only part of the references are listed.Craniosynostosis as a clinical and diagnostic problem: molecular pathology and genetic counseling
Anna Kutkowska-Kazmierczak et al.
JOURNAL OF APPLIED GENETICS (2018)
De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis
Andrew T. Timberlake et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)
Regulation of Calvarial Osteogenesis by Concomitant De-repression of GLI3 and Activation of IHH Targets
Lotta K. Veistinen et al.
FRONTIERS IN PHYSIOLOGY (2017)
Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosis
Jaclyn Greenwood et al.
GENETICS IN MEDICINE (2014)
Craniosynostosis
David Johnson et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2011)
Copy Number Variation Analysis in Single-Suture Craniosynostosis: Multiple Rare Variants Including RUNX2 Duplication in Two Cousins With Metopic Craniosynostosis
Heather C. Mefford et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2010)
Fetal Constraint as a Potential Risk Factor for Craniosynostosis
Pedro A. Sanchez-Lara et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2010)
Prevalence and Complications of Single-Gene and Chromosomal Disorders in Craniosynostosis
Andrew O. M. Wilkie et al.
PEDIATRICS (2010)
Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors
Anne Goriely et al.
NATURE GENETICS (2009)
Craniosynostosis: A Radiological and Surgical Perspective
Olga Kirmi et al.
SEMINARS IN ULTRASOUND CT AND MRI (2009)
A population-based study of craniosynostosis in metropolitan Atlanta, 1989-2003
Sheree L. Boulet et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
ChromaPipe: a pipeline for analysis, quality control and management for a DNA sequencing facility
T. D. Otto et al.
GENETICS AND MOLECULAR RESEARCH (2008)
High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation
F. S. Jehee et al.
JOURNAL OF MEDICAL GENETICS (2008)
Clinical dividends from the molecular genetic dincrnosis of craniosynostosis (vol 140, pg 2631, 2007)
Andrew O. M. Wilkie et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2007)
The origin of EFNB1 mutations in craniofrontonasal syndrome:: Frequent somatic mosaicism and explanation of the paucity of carrier males
Stephen R. F. Twigg et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Gain-of-function amino acid substitutions drive positive selection of FGFR2 mutations in human spermatogonia
A Goriely et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Share Paper
