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[PDF] from pucrs.brFP Varoli, KCP Santos… - … Ciência (Journal of …, 2011 - revistaseletronicas.pucrs.br
... usp.br Abstract Purpose: Apert syndrome is a rare type I acrocephalosyndactyly
syndrome characterized by craniosynostosis, severe syndactyly of the hands and
feet, and dysmorphic facial features. Presents autosomal dominant ...
Cited by 1 - Related articles - All 3 versions
宮脇剛司 - ペパーズ, 2011 - ci.nii.ac.jp
Cached
藤本卓也… - ペパーズ, 2011 - ci.nii.ac.jp
Cached
A Busche, LM Graul-Neumann, C Zweier… - European Journal of …, 2011 - Elsevier
... syndrome, TWIST1, deletion 7p21, blepharophimosis-ptosis-40 epicanthus inversus syndrome
41 42 43 44 45 46 47 48 49 50 51 52 MA NUSCRIPTACCEPTED ACCEPTED MANUSCRIPT
3 53 1. Introduction 54 Saethre-Chotzen syndrome or acrocephalosyndactyly type III ...
All 2 versions
[HTML] from ispub.comR Narang, S Sandhu, S Padda, J Sandhu… - The Internet Journal of …, 2011 - ispub.com
... 1. Acrocephalosyndactyly is a variant of craniosynostosis which is characterized by acrocephaly
and syndactyly of hands and feet often combined with anomalies of other organs. Some
investigators state that 4.5 percent of all craniosynostosis represent Apert syndrome. ...
Cached
[PDF] from pucrs.brFP Varoli, KCP Santos… - … Ciência (Journal of …, 2011 - revistaseletronicas.pucrs.br
... usp.br Abstract Purpose: Apert syndrome is a rare type I acrocephalosyndactyly
syndrome characterized by craniosynostosis, severe syndactyly of the hands and
feet, and dysmorphic facial features. Presents autosomal dominant ...
Cited by 1 - Related articles - All 3 versions
宮脇剛司 - ペパーズ, 2011 - ci.nii.ac.jp
Cached
藤本卓也… - ペパーズ, 2011 - ci.nii.ac.jp
Cached
A Busche, LM Graul-Neumann, C Zweier… - European Journal of …, 2011 - Elsevier
... syndrome, TWIST1, deletion 7p21, blepharophimosis-ptosis-40 epicanthus inversus syndrome
41 42 43 44 45 46 47 48 49 50 51 52 MA NUSCRIPTACCEPTED ACCEPTED MANUSCRIPT
3 53 1. Introduction 54 Saethre-Chotzen syndrome or acrocephalosyndactyly type III ...
All 2 versions
[HTML] from ispub.comR Narang, S Sandhu, S Padda, J Sandhu… - The Internet Journal of …, 2011 - ispub.com
... 1. Acrocephalosyndactyly is a variant of craniosynostosis which is characterized by acrocephaly
and syndactyly of hands and feet often combined with anomalies of other organs. Some
investigators state that 4.5 percent of all craniosynostosis represent Apert syndrome. ...
Cached

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