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6 in total

1. Atypical Crouzon syndrome with a novel Cys62Arg mutation in FGFR2 presenting with sagittal synostosis.

Authors: Vikram P Sharma; Steven A Wall; Helen Lord; Tracy Lester; Andrew O M Wilkie
Journal: Cleft Palate Craniofac J Date: 2011-11-25

2. Crouzon syndrome with acanthosis nigricans: a case-based update.

Authors: Federico Di Rocco; Corinne Collet; Laurence Legeai-Mallet; Eric Arnaud; Martine Le Merrer; Smail Hadj-Rabia; Dominique Renier
Journal: Childs Nerv Syst Date: 2010-12-07 Impact factor: 1.475

3. Crouzon syndrome with acanthosis nigricans: case report and mutational analysis.

Authors: T Nagase; M Nagase; S Hirose; K Ohmori
Journal: Cleft Palate Craniofac J Date: 2000-01

4. Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3.

Authors: D N Schweitzer; J M Graham; R S Lachman; E W Jabs; K Okajima; K A Przylepa; A Shanske; K Chen; J A Neidich; W R Wilcox
Journal: Am J Med Genet Date: 2001-01-01

Review 5. The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans.

Authors: Z Vajo; C A Francomano; D J Wilkin
Journal: Endocr Rev Date: 2000-02 Impact factor: 19.871

6. Crouzon with acanthosis nigricans. Further delineation of the syndrome.

Authors: L Arnaud-López; R Fragoso; J Mantilla-Capacho; P Barros-Núñez
Journal: Clin Genet Date: 2007-11 Impact factor: 4.438

6 in total