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The utility of molecular genetic techniques in craniosynostosis cases associated with intellectual disability Cover

The utility of molecular genetic techniques in craniosynostosis cases associated with intellectual disability

Revista Romana de Medicina de Laborator
Volume 26 (2018): Issue 4 (October 2018)
By: Alina Bogliş,  Florin Tripon and  Claudia Bănescu  
Open Access
|Oct 2018
DOI: https://doi.org/10.2478/rrlm-2018-0033 | Journal eISSN: 2284-5623 | Journal ISSN: 1841-6624
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Language: English
Page range: 471 - 477
Submitted on: Jul 29, 2018
|
Accepted on: Sep 18, 2018
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Published on: Oct 29, 2018
Published by: Romanian Association of Laboratory Medicine
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
Keywords:
craniosynostosis,
FGFR3,
Pro250Arg mutation,
MLPA analysis,
Sanger sequencing
Related subjects:
Life sciences,
Molecular biology,
Biochemistry,
Human biology,
Microbiology and virology

© 2018 Alina Bogliş, Florin Tripon, Claudia Bănescu, published by Romanian Association of Laboratory Medicine
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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