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Senturk, Leyli
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1

Clinical and molecular genetic findings of Crisponi/cold‐in..:

Yilmaz Gulec, Elif ; Turgut, Gozde Tutku ; Gezdirici, Alper...
Clinical Genetics.  102 (2022)  3 - p. 201-217 , 2022
Link: https://doi.org/10.1111/..
 
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2

Prenatal ultrasonographic features in Blomstrand osteochond..:

Sarac Sivrikoz, Tugba ; Kalayci, Tugba ; Senturk, Leyli...
Prenatal Diagnosis.  42 (2022)  12 - p. 1503-1510 , 2022
Link: https://doi.org/10.1002/..
 
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3

Heterozygous pathogenic variants inGLI1are a common finding..:

Palencia‐Campos, Adrián ; Martínez‐Fernández, María‐Luisa ; Altunoglu, Umut...
Human Mutation.  41 (2019)  1 - p. 265-276 , 2019
Link: https://doi.org/10.1002/..
 
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4

Kaufman oculocerebrofacial syndrome: Novel UBE3B mutations ..:

Yilmaz, Rüstem ; Szakszon, Katalin ; Altmann, Anna...
American Journal of Medical Genetics Part A.  176 (2017)  1 - p. 187-193 , 2017
Link: https://doi.org/10.1002/..
 
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5

Bartter Type 4a Syndrome Diagnosed in a 30-week-old Preterm..:

Çağrı Cumhur Gök ; Özge Kaynar ; Leyli Şentürk..
http://behmedicalbulletin.org/archives/archive-detail/article-preview/bartter-type-4a-syndrome-diagnosed-in-a-30-week-ol/58571.  , 2023
Link: https://doi.org/10.4274/..
 
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