Author/Creator: Cilingir, Oguz - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Cilingir, Oguz

1. A Turkish patient with novel AHCY variants and presumed diagnosis of S‐adenosylhomocysteine hydrolase deficiency. Issue 4 (20th January 2020)

Authors:: Bas, Hasan; Cilingir, Oguz; Tekin, Neslihan; Saylisoy, Suzan; Durak Aras, Beyhan; Uzay, Elif; Erzurumluoglu Gokalp, Ebru; Artan, Sevilhan
Journal:: American journal of medical genetics
Issue:: Volume 182:Issue 4(2020)
Page Start:: 740
Record Type:: Journal Article
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2. Apo E genotype and cerebral palsy. (June 2017)

Authors:: Gumus, Evren; Cilingir, Oguz; Yarar, Coskun; Carman, Kursat Bora; Ozdemir, Muhsin; Kocak, Ozan; Gurlevik, Sibel Lacinel; Artan, Sevlhan; Aras, Beyhan Durak
Journal:: European journal of paediatric neurology
Issue:: Volume 21(2017)Supplement 1
Page Start:: e72
Record Type:: Journal Article
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3. Clinical heterogeneity associated with TUBB3 gene mutation in a Turkish family with congenital fibrosis of the extraocular muscles. (4th May 2017)

Authors:: Ceylan, Ahmet Cevdet; Gursoy, Huseyin; Yildirim, Nilgun; Basmak, Hikmet; Erol, Nazmiye; Cilingir, Oguz
Journal:: Ophthalmic genetics
Issue:: Volume 38:Number 3(2017)
Page Start:: 288
Record Type:: Journal Article
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4. NDE1‐related disorders: A recurrent NDE1 pathogenic variant causing Lissencephaly 4 can also be associated with microhydranencephaly. Issue 1 (25th September 2021)

Authors:: Bas, Hasan; Saylisoy, Suzan; Cilingir, Oguz; Gokalp, Ebru Erzurumluoglu; Kocagil, Sinem; Yarar, Coskun; Aras, Beyhan Durak; Artan, Sevilhan
Journal:: American journal of medical genetics
Issue:: Volume 188:Issue 1(2022)
Page Start:: 326
Record Type:: Journal Article
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5. Prevalence of Nonclassic Congenital Adrenal Hyperplasia in Turkish Children Presenting with Premature Pubarche, Hirsutism, or Oligomenorrhoea. (23rd March 2014)

Authors:: Binay, Cigdem; Simsek, Enver; Cilingir, Oguz; Yuksel, Zafer; Kutlay, Ozden; Artan, Sevilhan
Other Names:: Castinetti Frederic Academic Editor.
Journal:: International journal of endocrinology
Issue:: Volume 2014(2014)
Page Start:
Record Type:: Journal Article
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6. The relationship of retinopathy of prematurity with brain-derivated neurotrophic factor, vascular endotelial growth factor-A, endothelial PAD domain protein 1 and nitric oxide synthase 3 gene polymorphisms. (2nd November 2021)

Authors:: Ilguy, Serdar; Cilingir, Oguz; Bilgec, Mustafa Deger; Ozalp, Onur; Erzurumluoglu Gokalp, Ebru; Arslan, Serap; Tekin, Neslihan; Aydemir, Ozge; Erol, Nazmiye; Colak, Ertugrul; Gursoy, Huseyin
Journal:: Ophthalmic genetics
Issue:: Volume 42:Number 6(2021)
Page Start:: 725
Record Type:: Journal Article
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