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Articles from Academic Databases : SCOPUS
Scopus 2019
Publication:
Novel mutation of the TINF2 gene resulting in severe phenotypic Revesz syndrome
Issued Date
2019-03-01
Resource Type
Letter
ISSN
15455017
15455009
DOI
10.1002/pbc.27557
Other identifier(s)
2-s2.0-85057450467
Rights
Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Pediatric Blood and Cancer. Vol.66, No.3 (2019)
Suggested Citation
APA
IEEE
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Chicago
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Anusak Sakwit, Duangnate Rojanaporn, Pimsiri Mekjaruskul, Wiboon Suriyajakryuththana, Werasak Sasanakul, Nongnuch Sirachainan
Novel mutation of the TINF2 gene resulting in severe phenotypic Revesz syndrome.
Pediatric Blood and Cancer. Vol.66, No.3 (2019).
doi:10.1002/pbc.27557
Retrieved from:
https://repository.li.mahidol.ac.th/handle/20.500.14594/51828
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Organizational Units
Authors
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Thesis
Title
Novel mutation of the TINF2 gene resulting in severe phenotypic Revesz syndrome
Author(s)
Anusak Sakwit
Duangnate Rojanaporn
Pimsiri Mekjaruskul
Wiboon Suriyajakryuththana
Werasak Sasanakul
Nongnuch Sirachainan
Other Contributor(s)
Faculty of Medicine, Ramathibodi Hospital, Mahidol University
Maharaj Nakhon Ratchasima Hospital
Keyword(s)
Medicine
Availability
URI
https://repository.li.mahidol.ac.th/handle/20.500.14594/51828
Collections
Scopus 2019
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