Ece Solmaz, Asli
75  results:
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1

A rare cause of primary amenorrhea: LHCGR gene mutations:

Aktar Karakaya, Amine ; Çayır, Atilla ; Unal, Edip...
European Journal of Obstetrics & Gynecology and Reproductive Biology.  272 (2022)  - p. 193-197 , 2022
 
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2

A novel bi-allelic variant in the SDHB gene causes a severe..:

Ece Solmaz, Asli ; Pariltay, Erhan ; Talim, Beril.
Clinical Neurology and Neurosurgery.  212 (2022)  - p. 107039 , 2022
 
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3

Mutation spectrum of the NF1 gene and genotype–phenotype co..:

Ece Solmaz, Asli ; Isik, Esra ; Atik, Tahir..
Clinical Neurology and Neurosurgery.  208 (2021)  - p. 106884 , 2021
 
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5

Targeted multi-gene panel testing for the diagnosis of Bard..:

Ece Solmaz, Asli ; Onay, Huseyin ; Atik, Tahir...
European Journal of Medical Genetics.  58 (2015)  12 - p. 689-694 , 2015
 
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7

20-year experience on prenatal diagnosis in a reference uni..:

DURMAZ, Burak ; BOLAT, Hilmi ; CENGİSİZ, Zehra...
TURKISH JOURNAL OF MEDICAL SCIENCES.  51 (2021)  4 - p. 1775-1780 , 2021
 
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11

Molecular spectrum of α-globin gene mutations in the Aegean..:

Onay, Hüseyin ; Aykut, Ayça ; Karaca, Emin...
International Journal of Hematology.  102 (2015)  1 - p. 1-6 , 2015
 
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