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Levent Şimşek
(Levent Simsek)
ORCID
Publication Activity (10 Years)
Years Active: 2019-2024
Publications (10 Years): 2
Top Topics
Intellectual Disability
Newly Diagnosed
Rare Case
Gene Expression
Top Venues
Biochemical genetics
Andrologia
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This page only lists publications with an associated author ORCID identifier.
Publications
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Özgür Balasar
,
Banu Kadıoğlu Yılmaz
,
Muserref Basdemirci
,
Hatice Koçak Eker
,
Büşra Eser Çavdartepe
,
Levent Şimşek
,
Ebru Tuncez
,
Fahrettin Duymuş
Assessment of Pathogenic Variants in the PAH Gene and Genotype-Phenotype Correlation in Phenylketonuria Patients from Turkey.
Biochemical genetics
(2024)
Levent Şimşek
,
Ayse Gul Zamani
,
Hakan Hakkı Taskapu
,
Mahmut Selman Yildirim
A rare case in literature: Isochromosome Xq in Klinefelter syndrome.
Andrologia
51 (5) (2019)