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1 . Academic Journal
Genetic Variations in Attention Deficit Hyperactivity Disorder Subtypes and Treatment Resistant Cases
저자
by
Unal, Dilek
;
Unal, Mehmet Fatih
;
Alikasifoglu, Mehmet
;
Cetinkaya, Arda
.
소스
Psychiatry Investigation
. 13(4):427-433
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6 . Academic Journal
Genetic disorders with symptoms mimicking rheumatologic diseases: A single-center retrospective study
저자
by
Kaya Akca, Ummusen
;
Simsek Kiper, Pelin Ozlem
;
Urel Demir, Gizem
;
Sag, Erdal
;
Atalay, Erdal
, et al.
소스
In
European Journal of Medical Genetics
April 2021 64(4)
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7 . Academic Journal
Intrafamilial variability of XYLT2-related spondyloocular syndrome
저자
by
Guleray, Naz
;
Simsek Kiper, Pelin Ozlem
;
Utine, Gulen Eda
;
Boduroglu, Koray
;
Alikasifoglu, Mehmet
.
소스
In
European Journal of Medical Genetics
November 2019 62(11)
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7 . Academic Journal
Hyperphosphatasia with mental retardation syndrome type 4 In two siblings-expanding the phenotypic and mutational spectrum
저자
by
Akgün Doğan, Özlem
;
Demir, Gizem Ürel
;
Kosukcu, Can
;
Taskiran, Ekim Z.
;
Simsek-Kiper, Pelin Özlem
, et al.
소스
In
European Journal of Medical Genetics
June 2019 62(6)
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7 . Academic Journal
A novel NKX3-2 mutation associated with perinatal lethal phenotype of spondylo-megaepiphyseal-metaphyseal dysplasia in a neonate
저자
by
Simsek-Kiper, Pelin Ozlem
;
Kosukcu, Can
;
Akgun-Dogan, Ozlem
;
Gocmen, Rahsan
;
Utine, Gulen Eda
, et al.
소스
In
European Journal of Medical Genetics
January 2019 62(1):21-26
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7 . Academic Journal
Fragile x-associated premature ovarian failure in a large Turkish cohort: Findings of Hacettepe Fragile X Registry
저자
by
Utine, Gülen Eda
;
Şimşek-Kiper, Pelin Özlem
;
Akgün-Doğan, Özlem
;
Ürel-Demir, Gizem
;
Alanay, Yasemin
, et al.
소스
In
European Journal of Obstetrics and Gynecology
February 2018 221:76-80
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7 . Academic Journal
HERC1 mutations in idiopathic intellectual disability
저자
by
Utine, G. Eda
;
Taşkıran, Ekim Z.
;
Koşukcu, Can
;
Karaosmanoğlu, Beren
;
Güleray, Naz
, et al.
소스
In
European Journal of Medical Genetics
May 2017 60(5):279-283
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7 . Academic Journal
CYP1A1 polymorphism in adolescents with polycystic ovary syndrome
저자
by
Akgül, Sinem
;
Derman, Orhan
;
Alikaşifoğlu, Mehmet
;
Aktaş, Dilek
.
소스
In
International Journal of Gynecology and Obstetrics
2011 112(1):8-10
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6 . Academic Journal
A case of Woodhouse-Sakati syndrome with pituitary iron deposition, cardiac and intestinal anomalies, with a novel mutation in DCAF17
저자
by
Sendur, Suleyman Nahit
;
Oguz, Sumeyra
;
Utine, Gulen Eda
;
Dagdelen, Selcuk
;
Oguz, Kader Karli
, et al.
소스
In
European Journal of Medical Genetics
August 2019 62(8)
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7 . Academic Journal
CYP1A1 gene polymorphism and polycystic ovary syndrome
저자
by
Esinler, Ibrahim
;
Aktas, Dilek
;
Otegen, Umit
;
Alikasifoglu, Mehmet
;
Yarali, Hakan
, et al.
소스
In
Reproductive BioMedicine Online
2008 16(3):356-360
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