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1 . Academic Journal
Asymptomatic hemochromatosis case with HFE c.1007−47G>A, c.340+4T>C heterozygous mutations and alpha globin −3.7 kb deletion
저자
by
Vesile Deniz Çelik
;
Betul Orhan Kiliç
;
Yasemin Ardiçoğlu Akişin
;
Fatma Ajlan Tükün
;
Nejat Akar
.
소스
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 4, Pp 433-435 (2018)
Full Text (ScienceDirect)
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7 .
Prognostic impact of RUNX1 and ETV6 gene copy number on pediatric B-cell precursor acute lymphoblastic leukemia with or without hyperdiploidy
저자
by
Elif İnce
;
Talia Ileri
;
Nuket Yurur Kutlay
;
Şule Altıner
;
Fatma Ajlan Tukun
, et al.
소스
International Journal of Hematology
. 104:368-377
Web of Science
Scopus
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7 .
Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents
저자
by
Cihan Topal
;
Korcan Demir
;
Özlem Nalbantoğlu
;
Selma Tunc
;
Fatma Ajlan Tükün
, et al.
소스
Journal of Clinical Research in Pediatric Endocrinology
Open Access (OpenAIRE)
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7 .
Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development
저자
by
Zeynep Şıklar
;
Şenay Savaş-Erdeve
;
Fatma Ajlan Tukun
;
Bülent Hacıhamdioğlu
;
Vehap Topcu
, et al.
소스
Journal of Pediatric Endocrinology and Metabolism
. 28
Scopus
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7 .
Asymptomatic hemochromatosis case with HFE c.1007?47G>A, c.340+4T>C heterozygous mutations and alpha globin ?3.7?kb deletion
저자
by
Yasemin Ardicoglu Akisin
;
Nejat Akar
;
Fatma Ajlan Tükün
;
Vesile Deniz Çelik
;
Betul Orhan Kiliç
, et al.
소스
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 4, Pp 433-435 (2018)
Open Access (OpenAIRE)
요약보기
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EndNote
RefWorks
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