Skip to main content
مکتبة رقمیه للعلوم الطبيه
Your cart is empty.
Cart
Lists
Your lists
Log in to create your own lists
Log in to your account
Your cookies
Search history
Search the catalog by:
Library catalog
Title
Author
Subject
ISBN
ISSN
Series
Call number
Search the catalog by keyword
Advanced search
Authority search
Tag cloud
Library
Log in to your account
Home
Advanced search
Results of search for 'au:"Tug, E"'
Refine your search
Availability
Limit to records with available items
Authors
Ahsen, H
Atasoy, H I
Aydin, H
Bakir, A
Baysoy, G
Bes, C
Boran, C
Cavdarli, B
Cine, N
De Paepe, A
Dogruer, D
Ergun, M A
Geckinli, B
Gideroglu, K
Guntekin, S
Kamanli, A
Karaoguz, M Yirmibes
Percin, F E
Tug, E
Tug, T
Show more
Show less
Topics
Abnormalities, Multiple
Adolescent
Adult
Asthma
Brain
Child
Chromosome Deletion
Chromosomes, Human, Pair 17
Craniofacial Abnormalities
Craniosynostoses
Female
Genetic Counseling
Haplotypes
Humans
Infant
Intellectual Disability
Male
Middle Aged
Young Adult
genetics
Show more
Show less
Languages
English
Your search returned 13 results.
Sort
Sort by:
Relevance
Popularity (most to least)
Popularity (least to most)
Author (A-Z)
Author (Z-A)
Call number (0-9 to A-Z)
Call number (Z-A to 9-0)
Publication/Copyright date: Newest to oldest
Publication/Copyright date: Oldest to newest
Acquisition date: Newest to oldest
Acquisition date: Oldest to newest
Title (A-Z)
Title (Z-A)
Unhighlight
Highlight
Select all
Clear all
Select titles to:
Add to cart
Add to list
New list
Place hold
Results
1.
Effects of long-term inhaled steroid use on bone mineral density in asthma patients.
[electronic resource]
by
Tug, T
Kamanli, A
Tug, E
Producer:
20021030
In:
Journal of investigational allergology & clinical immunology
vol. 11
Availability:
No items available.
Save to lists
Add to cart
(remove)
2.
A Turkish patient with large 17p11.2 deletion presenting with Smith Magenis syndrome.
[electronic resource]
by
Tug, E
Cine, N
Aydin, H
Producer:
20110711
In:
Genetic counseling (Geneva, Switzerland)
vol. 22
Availability:
No items available.
Save to lists
Add to cart
(remove)
3.
AN INTERCHANGE TRISOMY RESULTED IN DOWN SYNDROME.
[electronic resource]
by
Tug, E
Karaoguz, M Yirmibes
Bakir, A
Producer:
20181016
In:
Genetic counseling (Geneva, Switzerland)
vol. 27
Availability:
No items available.
Save to lists
Add to cart
(remove)
4.
Relationship between the IL-12B promoter polymorphism and allergic rhinitis, familial asthma, serum total IgE, and eosinophil level in asthma patients.
[electronic resource]
by
Tug, E
Ozbey, U
Tug, T
Yuce, H
Producer:
20090505
In:
Journal of investigational allergology & clinical immunology
vol. 19
Availability:
No items available.
Save to lists
Add to cart
(remove)
5.
Lack of an effect of CYP3A4 and MDR1 gene polymorphisms on colchicine pharmacogenetics in the treatment of Familial Mediterranean fever.
[electronic resource]
by
Dogruer, D
Tug, E
Bes, C
Soy, M
Producer:
20140408
In:
Genetics and molecular research : GMR
vol. 12
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
6.
The Impact of the D727E Polymorphism has no Significant Role in Multi Nodular Goiter.
[electronic resource]
by
Tug, E
Sengül, N
Aydin, H
Yilmaz, Ee
Producer:
20130920
In:
Balkan journal of medical genetics : BJMG
vol. 15
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
7.
MECP2 DUPLICATION SYNDROME WITH ADDITIONAL FINDINGS.
[electronic resource]
by
Tug, E
Ergun, M A
Percin, E F
Producer:
20181016
In:
Genetic counseling (Geneva, Switzerland)
vol. 27
Availability:
No items available.
Save to lists
Add to cart
(remove)
8.
Thrombophilia gene mutations in oculoauriculovertebral spectrum.
[electronic resource]
by
Tug, E
Atasoy, H I
Koybasi Sanal, S
Producer:
20120719
In:
Genetic counseling (Geneva, Switzerland)
vol. 23
Availability:
No items available.
Save to lists
Add to cart
(remove)
9.
Linkage analysis and a novel COL4A5 mutation in a large Turkish family with Alport syndrome.
[electronic resource]
by
Tug, E
Percin, F E
Pala, E
Baysoy, G
Producer:
20111013
In:
Genetic counseling (Geneva, Switzerland)
vol. 22
Availability:
No items available.
Save to lists
Add to cart
(remove)
10.
A patient with 9q subtelomeric deletion syndrome with additional findings.
[electronic resource]
by
Tug, E
Cavdarli, B
Karaoguz, M Yirmibes
Percin, F E
Producer:
20130404
In:
Genetic counseling (Geneva, Switzerland)
vol. 23
Availability:
No items available.
Save to lists
Add to cart
(remove)
11.
The evaluation of long-term effects of ionizing radiation through measurement of current sister chromatid exchange (SCE) rates in radiology technologists, compared with previous SCE values.
[electronic resource]
by
Tug, E
Kayhan, G
Kan, D
Guntekin, S
Ergun, M A
Producer:
20131211
In:
Mutation research
vol. 757
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
12.
A Turkish patient of typical Loeys-Dietz syndrome with a TGFBR2 mutation.
[electronic resource]
by
Tug, E
Loeys, B
De Paepe, A
Aydin, H
Gideroglu, K
Producer:
20100903
In:
Genetic counseling (Geneva, Switzerland)
vol. 21
Availability:
No items available.
Save to lists
Add to cart
(remove)
13.
Craniorachischisis, gastroschisis, and a branchial sinus defect: a case report.
[electronic resource]
by
Aydin, H
Yanik, S
Tug, E
Ahsen, H
Geckinli, B
Senol, S
Karaman, A
Yilmaz, F
Boran, C
Producer:
20140812
In:
Genetic counseling (Geneva, Switzerland)
vol. 25
Availability:
No items available.
Save to lists
Add to cart
(remove)