Poretti-Boltshauser syndrome : a rare differential diagnosis to consider in pediatric high myopia with retinal degeneration
Alahmadi, Adel Salah ; Badawi, Abdulrahman H. ; Magliyah, Moustafa S. ; Albakri, Amani and Schatz, Patrik LU
(2021)
In Ophthalmic Genetics
42(1).
p.96-98
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/b0362168-355f-438f-b7e2-7b118ab5dc0e
- author
- Alahmadi, Adel Salah
; Badawi, Abdulrahman H.
; Magliyah, Moustafa S.
; Albakri, Amani
and Schatz, Patrik
LU
- organization
- publishing date
- 2021
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Ophthalmic Genetics
- volume
- 42
- issue
- 1
- pages
- 96 - 98
- publisher
- Taylor & Francis
- external identifiers
-
- scopus:85096828946
- pmid:33251915
- ISSN
- 1381-6810
- DOI
- 10.1080/13816810.2020.1849316
- language
- English
- LU publication?
- yes
- id
- b0362168-355f-438f-b7e2-7b118ab5dc0e
- date added to LUP
- 2020-12-14 09:58:41
- date last changed
- 2024-04-03 18:47:27
@article{b0362168-355f-438f-b7e2-7b118ab5dc0e,
author = {{Alahmadi, Adel Salah and Badawi, Abdulrahman H. and Magliyah, Moustafa S. and Albakri, Amani and Schatz, Patrik}},
issn = {{1381-6810}},
language = {{eng}},
number = {{1}},
pages = {{96--98}},
publisher = {{Taylor & Francis}},
series = {{Ophthalmic Genetics}},
title = {{Poretti-Boltshauser syndrome : a rare differential diagnosis to consider in pediatric high myopia with retinal degeneration}},
url = {{http://dx.doi.org/10.1080/13816810.2020.1849316}},
doi = {{10.1080/13816810.2020.1849316}},
volume = {{42}},
year = {{2021}},
}