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Results of search for 'au:"Alikaşifoglu, M"', page 2 of 3
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Authors
Aktas, D
Aktaş, D
Alanay, Y
Alikasifoglu, M
Alikasifoğlu, M
Alikaşifoglu, M
Alikaşifoğlu, M
Altay, C
Anar, B
Arvas, A
Bakkaloglu, A
Besbas, N
Boduroglu, K
Boduroğlu, K
Ilter, O
Ozen, S
Tuncbilek, E
Tunçbilek, E
Unsal, I
Utine, G E
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Topics
Abnormalities, Multiple
Adolescent
Adult
Alleles
Case-Control Studies
Child
Child, Preschool
Educational Status
Female
Genetic Predisposition to Disease
Genotype
Humans
Infant
Infant, Newborn
Male
Polymorphism, Genetic
Turkey
diagnosis
epidemiology
genetics
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English
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21.
Bone density values in healthy Turkish infants.
[electronic resource]
by
Unal, A
Gur, E
Arvas, A
Erginel, A
Alikasifoglu, M
Ilter, O
Producer:
20010126
In:
Indian pediatrics
vol. 37
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No items available.
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22.
Tumor necrosis factor-alpha gene polymorphisms in children with multiple sclerosis.
[electronic resource]
by
Anlar, B
Alikaşifoglu, M
Köse, G
Güven, A
Gürer, Y
Yakut, A
Producer:
20011101
In:
Neuropediatrics
vol. 32
Online resources:
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23.
Influence of Bacillus Calmette-Guèrin vaccination at birth and 2 months old age on the peripheral blood T-cell subpopulations [gamma/delta and alpha-beta T cell].
[electronic resource]
by
Taştan, Y
Arvas, A
Demir, G
Alikaşifoğlu, M
Gür, E
Kiray, E
Producer:
20060131
In:
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
vol. 16
Online resources:
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24.
Factors influencing the duration of exclusive breastfeeding in a group of Turkish women.
[electronic resource]
by
Alikaşifoğlu, M
Erginoz, E
Gur, E T
Baltas, Z
Beker, B
Arvas, A
Producer:
20020607
In:
Journal of human lactation : official journal of International Lactation Consultant Association
vol. 17
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25.
Kabuki syndrome and trisomy 10p.
[electronic resource]
by
Utine, G E
Alanay, Y
Atkaş, D
Boduroğlu, K
Alikaşifoğlu, M
Tunçbilek, E
Producer:
20090123
In:
Genetic counseling (Geneva, Switzerland)
vol. 19
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26.
Allogeneic bone marrow transplantation in Fanconi anemia from Turkey: a report of four cases.
[electronic resource]
by
Tezcan, I
Tuncer, M
Uçkan, D
Cetin, M
Alikaşifoğlu, M
Ersoy, F
Altay, C
Producer:
19990413
In:
Pediatric transplantation
vol. 2
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27.
Polymorphisms in angiotensin converting enzyme gene and reflux nephropathy: a genetic predisposition to scar formation?
[electronic resource]
by
Ozen, S
Alikasifoglu, M
Tuncbilek, E
Bakkaloglu, A
Besbas, N
Aran, B
Saatci, U
Producer:
19971106
In:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
vol. 12
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28.
Analysis of 65 Turkish patients with congenital aplastic anemia (Fanconi anemia and non-Fanconi anemia): Hacettepe experience.
[electronic resource]
by
Altay, C
Alikaşifoglu, M
Kara, A
Tunçbilek, E
Ozbek, N
Schroeder-Kurth, T M
Producer:
19970819
In:
Clinical genetics
vol. 51
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29.
Clinical and genetic correlate in childhood onset Friedreich ataxia.
[electronic resource]
by
Alikaşifoglu, M
Topaloglu, H
Tunçbilek, E
Ceviz, N
Anar, B
Demir, E
Ozme, S
Producer:
19990818
In:
Neuropediatrics
vol. 30
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30.
Screening for the fragile X syndrome among mentally retarded males by hair root analysis.
[electronic resource]
by
Tunçbilek, E
Alikasifoğlu, M
Aktas, D
Duman, F
Yanik, H
Anar, B
Oostra, B
Willemsen, R
Producer:
20010104
In:
American journal of medical genetics
vol. 95
Online resources:
Available from publisher's website
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31.
Prevalence and persistence of hepatitis A antibody during the first year of life, in Turkish infants.
[electronic resource]
by
Alikasifoglu, M
Arvas, A
Tastan, Y
Tasdelen, E
Cullu, F
Ilter, O
Badur, S
Yüksel, D
Producer:
20000719
In:
Indian pediatrics
vol. 36
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32.
Natural immunity to Haemophilus influenzae type b among healthy children in Istanbul, Turkey.
[electronic resource]
by
Tastan, Y
Alikasifoglu, M
Ilter, O
Erginöz, E
Arvas, A
Yüksel, D
Türkcü, F
Badur, S
Producer:
20010112
In:
Indian pediatrics
vol. 37
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33.
Comparison study of the immunogenicity of different types and dosages of recombinant hepatitis B vaccine in healthy neonates.
[electronic resource]
by
Alikaşifoğlu, M
Cullu, F
Kutlu, T
Arvas, A
Taştan, Y
Erginöz, E
Kaypmaz, A
Tümay, G
Producer:
20010405
In:
Journal of tropical pediatrics
vol. 47
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34.
Tumour necrosis factor alpha G-->A -238 and G-->A -308 polymorphisms in juvenile idiopathic arthritis.
[electronic resource]
by
Ozen, S
Alikasifoglu, M
Bakkaloglu, A
Duzova, A
Jarosova, K
Nemcova, D
Besbas, N
Vencovsky, J
Tuncbilek, E
Producer:
20020418
In:
Rheumatology (Oxford, England)
vol. 41
Online resources:
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35.
Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability.
[electronic resource]
by
Utine, G E
Kiper, P Ö
Alanay, Y
Haliloğlu, G
Aktaş, D
Boduroğlu, K
Tunçbilek, E
Alikaşifoğlu, M
Publication details:
Molecular syndromology
Jan 2012
In:
Molecular syndromology
vol. 2
Online resources:
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36.
Assessment of whole-brain white matter by DTI in autosomal recessive spastic ataxia of Charlevoix-Saguenay.
[electronic resource]
by
Oguz, K K
Haliloglu, G
Temucin, C
Gocmen, R
Has, A C
Doerschner, K
Dolgun, A
Alikasifoglu, M
Producer:
20140527
In:
AJNR. American journal of neuroradiology
vol. 34
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37.
Methylene tetrahydrofolate reductase genotype and the risk and extent of coronary artery disease in a population with low plasma folate.
[electronic resource]
by
Tokgözoğlu, S L
Alikaşifoğlu, M
Atalar, E
Aytemir, K
Ozer, N
Ovünç, K
Usal, O
Kes, S
Tunçbilek, E
Producer:
19990603
In:
Heart (British Cardiac Society)
vol. 81
Online resources:
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38.
Opinions of Turkish physicians towards termination of pregnancy for fetal disorders.
[electronic resource]
by
Utine, G E
Kiper, P O
Salanci, B V
Alanay, Y
Aktaş, D
Alikaşifoğlu, M
Boduroğlu, K
Tunçbilek, E
Producer:
20120306
In:
Genetic counseling (Geneva, Switzerland)
vol. 22
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39.
Café noir spots: a feature of familial progressive hyper- and hypopigmentation.
[electronic resource]
by
Gülseren, D
Güleray, N
Akgün-Doğan, Ö
Şimşek-Kiper, P Ö
Utine, E G
Alikaşifoğlu, M
Ersoy-Evans, S
Producer:
20201123
In:
Journal of the European Academy of Dermatology and Venereology : JEADV
vol. 34
Online resources:
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40.
Implications of certain genetic polymorphisms in scarring in vesicoureteric reflux: importance of ACE polymorphism.
[electronic resource]
by
Ozen, S
Alikasifoglu, M
Saatci, U
Bakkaloglu, A
Besbas, N
Kara, N
Kocak, H
Erbas, B
Unsal, I
Tuncbilek, E
Producer:
19990726
In:
American journal of kidney diseases : the official journal of the National Kidney Foundation
vol. 34
Online resources:
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