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1 . Academic Journal
Looking for timing variations in the transits of 16 exoplanets.
저자
by
Yalçınkaya, S
;
Esmer, E M
;
Baştürk, Ö
;
Muhaymin, A
;
Kutluay, A C
, et al.
소스
Monthly Notices of the Royal Astronomical Society
. May2024, Vol. 530 Issue 3, p2475-2495. 21p.
Open Access (OUP)
Web of Science
Scopus
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7 . Academic Journal
Transit timing variation analysis of the low-mass brown dwarf KELT-1 b.
저자
by
Baştürk, Ö
;
Southworth, J
;
Yalçınkaya, S
;
Mancini, L
;
Esmer, E M
, et al.
소스
Monthly Notices of the Royal Astronomical Society
. May2023, Vol. 521 Issue 1, p1200-1209. 10p.
Open Access (OUP)
Web of Science
Scopus
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7 .
Relationship between periparturient diseases, metabolic markers and the dynamics of hair cortisol concentrations in dairy cows
저자
by
Tekin, M
;
Câmara, D R
;
Binz, T M
;
Bruckmaier, R M
;
Bollwein, H
, et al.
소스
Research in Veterinary Science
. 158:134-140
Open Access (OpenAIRE)
Web of Science
Scopus
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7 . Academic Journal
Evaluation of the academic productivity of the top 100 worldwide physicians in the field of otorhinolaryngology and head and neck surgery using the Google Scholar h-index as the bibliometrics ranking system.
저자
by
Kalcioglu, M T
;
Ileri, Y
;
Ozdamar, O I
;
Yilmaz, U
;
Tekin, M
.
소스
Journal of Laryngology & Otology
. Dec2018, Vol. 132 Issue 12, p1097-1101. 5p.
Web of Science
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7 . Academic Journal
Prevalence and mutations of β-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey.
저자
by
Uludağ, A
;
Uysal, A
;
Ertekin, YH
;
Tekin, M
;
Kütük, B
, et al.
소스
Balkan Journal of Medical Genetics
. Jul2016, Vol. 19 Issue 1, p29-34. 6p.
Web of Science
Scopus
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7 . Periodical
The MEFVgene pathogenic variants and phenotype-genotype correlation in children with familial Mediterranean fever in the Çanakkale population
저자
by
Battal, F
;
Silan, F
;
Topaloğlu, N
;
Aylanç, H
;
Yıldırım, Ş
, et al.
소스
Balkan Journal of Medical Genetics; December 2016, Vol. 19 Issue: 2 p23-28, 6p
Web of Science
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7 . Academic Journal
A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss
저자
by
Yariz, K O
;
Walsh, T
;
Akay, H
;
Duman, D
;
Akkaynak, A C
, et al.
소스
Clinical Genetics
. Mar 01, 2012 81(3):289-293
Web of Science
Scopus
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7 . Academic Journal
AUTOZYGOSITY SEARCH IN A TURKISH FAMILY WITH SCOLIOSIS, BLINDNESS, AND ARACHNODACTYLY: B05
저자
by
Orenay, S
;
Tekin, M
;
Dundar, M
.
소스
Clinical Genetics
. Nov 01, 2010 78 Suppl 1:43-43
Web of Science
Scopus
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5 . Academic Journal
A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia
저자
by
Srmac, A
;
Öztürkmen-Akay, H
;
Erbek, S
;
İncesulu, A
;
Duman, D
, et al.
소스
Clinical Genetics
. Jun 01, 2009 75(6):562-567
Web of Science
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7 . Academic Journal
Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey.
저자
by
Tekin, M
;
Akçayöz, D
;
Çomak, E
;
Boğoçlu, G
;
Duman, T
, et al.
소스
Clinical Genetics
. Oct2003, Vol. 64 Issue 4, p371. 4p.
Web of Science
Scopus
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