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February 18, 2012
Thyroglossal duct cysts: evaluation and treatment of 49 cases
H Yaman, A Durmaz, H H Arslan, et al.
Genetic Counseling (Geneva, Switzerland)
|
September 17, 2013
Subtelomeric rearrangements in patients with idiopathic intellectual disabilitiy/ multiple congenital anomalies and recurrent miscarriages: seven years' experience
B Durmaz, E Karaca, A Durmaz, et al.
Zeitschrift Fur Rheumatologie
|
October 22, 2016
The effects of high serum growth hormone and IGF-1 levels on bone mineral density in acromegaly
S Tuzcu, Ş A Durmaz, A Carlıoğlu, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 26, 2014
Genome-wide copy number variation analysis in idiopathic intellectual disability/multiple congenital anomalies
E Pariltay, A Durmaz, B Durmaz, et al.
The Journal of Cell Biology
|
June 20, 2025
ALDH9A1 deficiency as a source of endogenous DNA damage that requires repair by the Fanconi anemia pathway
Moonjung Jung, Jungwoo Kim, Yeji Park, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
B-ENT
|
February 18, 2012
Thyroglossal duct cysts: evaluation and treatment of 49 cases
H Yaman, A Durmaz, H H Arslan, et al.
Genetic Counseling (Geneva, Switzerland)
|
September 17, 2013
Subtelomeric rearrangements in patients with idiopathic intellectual disabilitiy/ multiple congenital anomalies and recurrent miscarriages: seven years' experience
B Durmaz, E Karaca, A Durmaz, et al.
Zeitschrift Fur Rheumatologie
|
October 22, 2016
The effects of high serum growth hormone and IGF-1 levels on bone mineral density in acromegaly
S Tuzcu, Ş A Durmaz, A Carlıoğlu, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 26, 2014
Genome-wide copy number variation analysis in idiopathic intellectual disability/multiple congenital anomalies
E Pariltay, A Durmaz, B Durmaz, et al.
The Journal of Cell Biology
|
June 20, 2025
ALDH9A1 deficiency as a source of endogenous DNA damage that requires repair by the Fanconi anemia pathway
Moonjung Jung, Jungwoo Kim, Yeji Park, et al.
Page
of 2