Identification of a genetic cause for isolated unilateral coronal synostosis: A unique mutation in the fibroblast growth factor receptor 3-Reference-Cited by-同舟云学术

Identification of a genetic cause for isolated unilateral coronal synostosis: A unique mutation in the fibroblast growth factor receptor 3

Published:1998-04 Issue:4 Volume:132 Page:714-716
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Gripp Karen W.,McDonald-McGinn Donna M.,Gaudenz Karin,Whitaker Linton A.,Bartlett Scott P.,Glat Paul M.,Cassileth Lisa B.,Mayro Rosario,Zackai Elaine H.,Muenke Maximilian

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference15 articles.

1. Association between “plagiocephaly” and hemifacial microsomia;Padwa;Am J Med Genet,1993

2. Observations on a recent increase in plagiocephaly without synostosis;Kane;Pediatrics,1996

3. Frontal plagiocephaly: synostotic, compensational, or deformational;Bruneteau;Plast Reconstr Surg,1992

4. Coronal craniostenosis: fetal head constraint as one possible cause;Graham;Pediatrics,1980

5. Intrauterine constraint and craniosynostosis;Higginbottom;Neurosurgery,1980

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