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Metin Eser
Specialist
UNIVERSITY OF HEALTH SCIENCES, İSTANBUL ÜMRANİYE HEALTH RESEARCH CENTER, DEPARTMENT OF INTERNAL MEDICINE, DEPARTMENT OF MEDICAL GENETICS
Publication
3
Review
0
CrossRef Cited
1
3
Publication
0
Review
1
CrossRef Cited
0000-0001-7118-7958
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Summary
Publications
Peer Review
Cited
Research Fields
Developmental Genetics
Institution
UNIVERSITY OF HEALTH SCIENCES, İSTANBUL ÜMRANİYE HEALTH RESEARCH CENTER, DEPARTMENT OF INTERNAL MEDICINE, DEPARTMENT OF MEDICAL GENETICS
Publications
Myotonia may be a sign that prompts genetic testing for myotonic dystrophy type 1
Authors:
Metin Eser
,
Gulam Hekimoğlu
,
Büşra Kutlubay
Published: 2025 ,
The European Research Journal
DOI: 10.18621/eurj.1553885
FAVORITE
0
TOTAL DOWNLOAD COUNT
104
0
FAVORITE
104
TOTAL DOWNLOAD COUNT
X-Linked Intellectual Disability with NEXMIF Gene Mutation and Developmental Delay with GNAO1 Gene Mutation: Case Report
Authors:
Tayfun Aygün
,
Sevim Yener
,
Nurullah Yücel
,
Gulam Hekimoğlu
,
Metin Eser
,
Zekeriya İlce
Published: 2024 ,
Medical Research Reports
DOI: 10.55517/mrr.1439712
FAVORITE
0
TOTAL DOWNLOAD COUNT
170
0
FAVORITE
170
TOTAL DOWNLOAD COUNT
Epidemiological Evaluation of Next-Generation Sequencing and MLPA Results in Patients with a Presumptive Cystic Fibrosis Diagnosis
Authors:
Sezin Canbek
,
Murat Hakkı Yarar
,
Metin Eser
,
Hakan Yazan
Published: 2024 ,
Osmangazi Tıp Dergisi
DOI: 10.20515/otd.1482361
FAVORITE
0
TOTAL DOWNLOAD COUNT
413
0
FAVORITE
413
TOTAL DOWNLOAD COUNT
Articles published in
Medical Research Reports
Osmangazi Tıp Dergisi
The European Research Journal
User doesn't have any peer review duties on DergiPark.
Publications
X-Linked Intellectual Disability with NEXMIF Gene Mutation and Developmental Delay with GNAO1 Gene Mutation: Case Report
Authors:
Tayfun Aygün
,
Sevim Yener
,
Nurullah Yücel
,
Gulam Hekimoğlu
,
Metin Eser
,
Zekeriya İlce
Published: 2024 ,
Medical Research Reports
DOI: 10.55517/mrr.1439712
CITED
1
FAVORITE
0
TOTAL DOWNLOAD COUNT
170
1
CITED
0
FAVORITE
170
TOTAL DOWNLOAD COUNT
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