The identification and characterisation of disease genes in craniosynostosis
<p>Current challenges to the understanding and clinical management of craniosynostosis (premature fusion of the cranial sutures) include the interpretation of changes in known disease genes, the identification of novel disease genes and the identification of pathogenic regulatory mutations. Th...
Κύριος συγγραφέας: | Fenwick, AL |
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Άλλοι συγγραφείς: | Wilkie, AOM |
Μορφή: | Thesis |
Γλώσσα: | English |
Έκδοση: |
2015
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Θέματα: |
Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
-
The clinical management of craniosynostosis /
ανά: Hayward, Richard
Έκδοση: (2004) -
Diagnóstico y evolución de un paciente con acrocefalosindactilia tipo I o síndrome de Apert
ανά: Milvia Castillo Guerrero, κ.ά.
Έκδοση: (2017-02-01) -
Pembangunan sistem perolehan imej fotogrametri digital jarak dekat bagi pengukuran craniofacial /
ανά: Mohd. Farid Mohd. Ariff
Έκδοση: (2005) -
Pembangunan sistem perolehan imej fotogrametri digital jarak dekat bagi pengukuran craniofacial [compact disc] /
ανά: Mohd. Farid Mohd. Ariff
Έκδοση: (2005) -
Non-syndromic craniosynostosis: a retrospective
analysis
ανά: Murilo Sgarbi Secanho, κ.ά.
Έκδοση: (2020-12-01)