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1 . Academic Journal
PB2657: DIFFERENT TYPES OF LEUKEMIAS AND BLEEDING DISORDER DETECTED IN A TURKISH FAMILY WITH GERMLINE RUNX1 MUTATION FOR THE FIRST TIME.
저자
by
Pinar Ata
;
Şenol Demir
;
Fatma Arikan
;
Tayfur Toptas
;
Ahmet Arman
.
소스
HemaSphere, Vol 7, p e96979d7 (2023)
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7 . Academic Journal
Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity
저자
by
Serap Turan
;
Steven Mumm
;
Ceren Alavanda
;
Betul Sare Kaygusuz
;
Busra Gurpinar Tosun
, et al.
소스
JBMR Plus, Vol 6, Iss 8, Pp n/a-n/a (2022)
Open Access (Wiley)
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7 . Academic Journal
O polimorfismo VNTR no gene codificador do antagonista do receptor da interleucina-1 está associado com a doença arterial coronariana Interleukin-1 receptor antagonist gene VNTR polymorphism is associated with coronary artery disease
저자
by
Ahmet Arman
;
Ozer Soylu
;
Ahmet Yildirim
;
Andrzej Furman
;
Nesrin Ercelen
, et al.
소스
Arquivos Brasileiros de Cardiologia, Vol 91, Iss 5, Pp 293-298 (2008)
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Scopus
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7 .
Novel, homozygous RAB3GAP1 c.2606 + 1G>A, p.Glu830ValfsTer9 variant and chromosome 3q29 duplication in a Turkish individual with Warburg micro syndrome
저자
by
Bilge Geckinli
;
Ayberk Turkyilmaz
;
Ceren Alavanda
;
Gunes Sager
;
Esra Arslan Ates
, et al.
소스
Clinical Dysmorphology
. 32:55-61
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7 .
Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty
저자
by
Tarık Kırkgöz
;
Sare Betül Kaygusuz
;
Ceren Alavanda
;
Didem Helvacıoğlu
;
Zehra Yavaş Abalı
, et al.
소스
Journal of Pediatric Endocrinology and Metabolism
.
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7 .
Two new cases with novel pathogenic variants reflecting the clinical diversity of
Schaaf‐Yang
syndrome
저자
by
Ceren Alavanda
;
Esra Arslan Ateş
;
Zehra Yavaş Abalı
;
Bilgen Bilge Geçkinli
;
Serap Turan
, et al.
소스
Clinical Genetics
.
Open Access (OpenAIRE)
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7 .
Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency
저자
by
Ayberk Turkyilmaz
;
Ceren Alavanda
;
Esra Arslan Ates
;
Bilgen Bilge Geckinli
;
Hamza Polat
, et al.
소스
J Assist Reprod Genet
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7 .
First patient diagnosed as feingold syndrome type 2 with alport syndrome and review of the current literature
저자
by
Şenol Demir
;
Mehmet A. Söylemez
;
Ahmet Arman
;
Pınar Ata
;
Demir S., SÖYLEMEZ M. A., ARMAN A., ATA P.
.
소스
Mol Syndromol
Open Access (OpenAIRE)
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7 .
Meckel-Gruber Syndrome: Clinical and Molecular Genetic Profiles in Two Fetuses and Review of the Current Literature
저자
by
Ceren Alavanda
;
Sirin Funda Eren
;
Ayberk Turkyilmaz
;
Esra Arslan Ates
;
Esra Esim Büyükbayrak
, et al.
소스
Genetic Testing and Molecular Biomarkers
. 25:445-451
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7 .
Vitamin D receptor gene polymorphisms in pediatric patients with leukemia-lymphoma: Does it have an impact on malignancy?
저자
by
Sinem GULCAN KERSIN
;
Ayse Gulnur TOKUC
;
Ahmet ARMAN
;
Baris YILMAZ
.
소스
Volume: 35, Issue: 3 270-274
Marmara Medical Journal
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