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1 . Academic Journal
Konjenital Anomali ve/veya Nörogelişimsel Geriliği olan Çocukluk Çağındaki Türk Hastalarda Kromozomal Mikroarray Deneyimi: ASXL2 Gen Duplikasyonu ve Xq13 Delesyonunun İncelenmesi.
저자
by
Unal, Aysel Tekmenuray
;
Durmaz, Ceren Damla
.
소스
Dicle Medical Journal / Dicle Tip Dergisi
. Mar2024, Vol. 51 Issue 1, p135-148. 14p.
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4 . Academic Journal
FBLN5-Related Cutis Laxa Syndrome: A Case with a Novel Variant and Review of the Literature.
저자
by
Tekmenuray-Unal, Aysel
;
Durmaz, Ceren Damla
.
소스
Molecular Syndromology; 2023, Vol. 14 Issue 1, p80-88, 8p
Scopus
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4 . Academic Journal
Genetic Analysis of RASD1 as a Candidate Gene for Schizophrenia.
저자
by
Durmaz, Ceren Damla
;
Karabulut, Halil Gürhan
;
Saka, Meram Can
;
Sucularlı, Ceren
;
Akay, Güvem Gümüş
, et al.
소스
Balkan Medical Journal
. Nov2022, Vol. 39 Issue 6, p422-428. 7p.
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7 . Academic Journal
Phenotypic and molecular characterization of five patients with PIK3CA‐related overgrowth spectrum (PROS).
저자
by
Gökpınar İli, Ezgi
;
Taşdelen, Elifcan
;
Durmaz, Ceren Damla
;
Altıner, Şule
;
Tuncalı, Timur
, et al.
소스
American Journal of Medical Genetics. Part A; Jun2022, Vol. 188 Issue 6, p1792-1800, 9p
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7 . Academic Journal
Undifferentiated Melanoma Resembling Undifferentiated Round Cell Sarcoma: The Diagnostic Power of Molecular Melanoma Signature.
저자
by
Kavuncuoglu, Altan
;
Durmaz, Ceren Damla
;
Gokoz, Ozay
;
Uner, Aysegul
;
Kosemehmetoglu, Kemal
.
소스
International Journal of Surgical Pathology
. May2022, Vol. 30 Issue 3, p346-349. 4p.
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7 . Academic Journal
Extending Phenotypic Spectrum of 17q22 Microdeletion: Growth Hormone Deficiency.
저자
by
Durmaz, Ceren Damla
;
Altıner, Şule
;
Taşdelen, Elifcan
;
Karabulut, Halil Gürhan
;
Ruhi, Hatice Ilgın
.
소스
Fetal & Pediatric Pathology
. October 2021, Vol. 40 Issue 5, p486-492. 7p.
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7 . Academic Journal
MASP1‐related 3MC syndrome in a patient from Turkey.
저자
by
Durmaz, Ceren Damla
;
Altıner, Şule
.
소스
American Journal of Medical Genetics. Part A; Jul2021, Vol. 185 Issue 7, p2267-2270, 4p
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4 . Academic Journal
Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the GLI2 Gene.
저자
by
Demiral, Meliha
;
Demirbilek, Hüseyin
;
Unal, Edip
;
Durmaz, Ceren Damla
;
Ceylaner, Serdar
, et al.
소스
Journal of Clinical Research in Pediatric Endocrinology
. Sep2020, Vol. 12 Issue 3, p319-328. 10p.
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7 . Academic Journal
Extending Phenotypic Spectrum of 17q22 Microdeletion: Growth Hormone Deficiency
저자
by
Durmaz, Ceren Damla
;
Altiner, Sule
;
Tasdelen, Elifcan
;
Karabulut, Halil Gurhan
;
Ruhi, Hatice Ilgin
.
소스
FETAL AND PEDIATRIC PATHOLOGY
; JAN 28 2020, 7p.
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7 .
Bilateral choanal atresia in an adult woman with pycnodysostosis
저자
by
Durmaz, Ceren Damla
;
Tas, Vedat
;
Kocaay, Pinar
;
Fitoz, Omer Suat
;
Onay, Huseyin
, et al.
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