Germinal mosaicism in Crouzon syndrome. A family with three affected siblings of normal parents

2008 ◽  
Vol 40 (1) ◽  
pp. 29-34 ◽  
Author(s):  
Carmen Navarrete ◽  
Ramón Peña ◽  
Rosenda Peñaloza ◽  
Fabio Salamanca
Keyword(s):  
Crouzon Syndrome ◽  
Germinal Mosaicism

Germinal mosaicism in Crouzon syndrome

2008 ◽  
Vol 33 (3) ◽  
pp. 145-150 ◽  
Author(s):  
B. R. Rollnick
Keyword(s):  
Crouzon Syndrome ◽  
Germinal Mosaicism

Germinal mosaicism in Crouzon syndrome

1990 ◽  
Vol 84 (5) ◽  
pp. 487-488 ◽  
Author(s):  
Sven Kreiborg ◽  
M. Michael Cohen
Keyword(s):  
Crouzon Syndrome ◽  
Germinal Mosaicism

Germinal mosaicism in a Duchenne muscular dystrophy family: implications for genetic counselling

2008 ◽  
Vol 43 (5) ◽  
pp. 247-249 ◽  
Author(s):  
Maria Antonietta Melis ◽  
Milena Cau ◽  
Rita Congiu ◽  
Rosalha Puddu ◽  
Francesco Muntoni ◽  
...  
Keyword(s):  
Duchenne Muscular Dystrophy ◽  
Muscular Dystrophy ◽  
Genetic Counselling ◽  
Germinal Mosaicism

scholarly journals Crouzon Syndrome: a case report

2010 ◽  
Vol 3 (S1) ◽  
Author(s):  
David Reid ◽  
Stuart Morrison
Keyword(s):  
Case Report ◽  
Crouzon Syndrome

Crouzon Syndrome: Relationship of Eye Movements to Pattern Strabismus

2015 ◽  
Vol 56 (8) ◽  
pp. 4394 ◽  
Author(s):  
Avery H. Weiss ◽  
John P. Kelly ◽  
Richard A. Hopper ◽  
James O. Phillips
Keyword(s):  
Eye Movements ◽  
Crouzon Syndrome ◽  
Relationship Of

The Spheno-Occipital Synchondrosis Fuses Prematurely in Patients With Crouzon Syndrome and Midface Hypoplasia Compared With Age- and Gender-Matched Controls

2014 ◽  
Vol 72 (6) ◽  
pp. 1173-1179 ◽  
Author(s):  
Youssef Tahiri ◽  
J. Thomas Paliga ◽  
Arastoo Vossough ◽  
Scott P. Bartlett ◽  
Jesse A. Taylor
Keyword(s):  
Crouzon Syndrome ◽  
Age And Gender ◽  
Midface Hypoplasia ◽  
And Gender

A Novel FGFR2 Gene Mutation in Crouzon Syndrome Associated with Apparent Nonpenetrance

1999 ◽  
Vol 36 (6) ◽  
pp. 533-541 ◽  
Author(s):  
Eric T. Everett ◽  
Denis A. Britto ◽  
Richard E. Ward ◽  
James K. Hartsfield
Keyword(s):  
Gene Mutation ◽  
Crouzon Syndrome ◽  
Fgfr2 Gene

scholarly journals Lack of association of cranial lacunae with intracranial hypertension in children with Crouzon syndrome and Apert syndrome: a 3D morphometric quantitative analysis

2019 ◽  
Vol 35 (3) ◽  
pp. 501-507
Author(s):  
Ankita Mondal ◽  
Naiara Rodriguez-Florez ◽  
Justine O’Hara ◽  
Juling Ong ◽  
N. u. Owase Jeelani ◽  
...  
Keyword(s):  
Quantitative Analysis ◽  
Intracranial Hypertension ◽  
Apert Syndrome ◽  
Crouzon Syndrome ◽  
Hypertension In Children
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