[HTML][HTML] Saethre–Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome
W Kress, C Schropp, G Lieb, B Petersen… - European Journal of …, 2006 - nature.com
Abstract The Saethre–Chotzen syndrome (SCS) is an autosomal dominant craniosynostosis
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …
[PDF][PDF] Saethre–Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome
W Kress, C Schropp, G Lieb, B Petersen… - European Journal of …, 2005 - academia.edu
The Saethre–Chotzen syndrome (SCS) is an autosomal dominant craniosynostosis
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …
[引用][C] Saethre–Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome
W Kress, C Schropp, G Lieb, B Petersen… - European Journal of …, 2005 - cir.nii.ac.jp
Saethre–Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from
Muenke coronal synostosis syndrome | CiNii Research CiNii 国立情報学研究所 学術情報 …
Muenke coronal synostosis syndrome | CiNii Research CiNii 国立情報学研究所 学術情報 …
Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.
W Kress, C Schropp, G Lieb, B Petersen… - European Journal of …, 2006 - europepmc.org
The Saethre-Chotzen syndrome (SCS) is an autosomal dominant craniosynostosis
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …
[引用][C] Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from muenke coronal synostosis syndrome
W KRESS, C SCHROPP, J PAHNKE… - European journal of …, 2006 - pascal-francis.inist.fr
Saethre-Chotzen syndrome caused by TWIST 1 gene mutations : functional differentiation
from muenke coronal synostosis syndrome CNRS Inist Pascal-Francis CNRS Pascal and …
from muenke coronal synostosis syndrome CNRS Inist Pascal-Francis CNRS Pascal and …
Saethre–Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.
W Kress, C Schropp, G Lieb… - … Journal of Human …, 2006 - search.ebscohost.com
Abstract The Saethre–Chotzen syndrome (SCS) is an autosomal dominant craniosynostosis
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …
Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome
W Kress, C Schropp, G Lieb… - … journal of human …, 2006 - pubmed.ncbi.nlm.nih.gov
The Saethre-Chotzen syndrome (SCS) is an autosomal dominant craniosynostosis
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …
[PDF][PDF] Saethre–Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome
W Kress, C Schropp, G Lieb, B Petersen… - European Journal of …, 2005 - researchgate.net
The Saethre–Chotzen syndrome (SCS) is an autosomal dominant craniosynostosis
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …
Saethre–Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.
W Kress, C Schropp, G Lieb… - … Journal of Human …, 2006 - search.ebscohost.com
Abstract The Saethre–Chotzen syndrome (SCS) is an autosomal dominant craniosynostosis
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …
syndrome with uni-or bilateral coronal synostosis and mild limb deformities. It is caused by …