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Results of search for 'au:"Aktaş, D"', page 1 of 2
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Authors
Aktas, D
Aktaş, D
Alanay, Y
Alikasifoglu, M
Alikasifoğlu, M
Alikaşifoğlu, M
Anar, B
Ayhan, A
Balci, S
Boduroglu, K
Boduroğlu, K
Cetin, M
Haliloğlu, G
Hicsonmez, G
Koç, A
Liehr, T
Mrasek, K
Tuncbilek, E
Tunçbilek, E
Utine, G E
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Topics
Abnormalities, Multiple
Adolescent
Adult
Case-Control Studies
Child
Child, Preschool
Chromosome Aberrations
Female
Fragile X Syndrome
Humans
Intellectual Disability
Karyotyping
Male
Middle Aged
Mosaicism
Myelodysplastic Syndromes
Trisomy
Turkey
diagnosis
genetics
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English
g d
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1.
Mucinous carcinoma of the colon in a 16-year-old Turkish boy with Bloom syndrome: cytogenetic, histopathologic, TP53 gene and protein expression studies.
[electronic resource]
by
Balci, S
Aktas, D
Producer:
19990526
In:
Cancer genetics and cytogenetics
vol. 111
Online resources:
Available from publisher's website
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2.
The relationship between traumatic tympanic membrane perforations and pneumatization of the mastoid.
[electronic resource]
by
Aktaş, D
Kutlu, R
Producer:
20010531
In:
ORL; journal for oto-rhino-laryngology and its related specialties
vol. 62
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3.
Mosaicism for terminal deletion of 4q.
[electronic resource]
by
Utine, G E
Aktas, D
Producer:
20061228
In:
Genetic counseling (Geneva, Switzerland)
vol. 17
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4.
Chromosomal mosaicism in a pregnant woman treated with acyclovir for herpes simplex encephalitis.
[electronic resource]
by
Aktas, D
Tuncbilek, E
Onderoglu, L
Producer:
20011204
In:
American journal of perinatology
vol. 18
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5.
Loss of maternal allele in a child with myelodysplastic syndrome and monosomy 7.
[electronic resource]
by
Aktas, D
Yenicesu, I
Hicsonmez, G
Tuncbilek, E
Producer:
19990930
In:
American journal of hematology
vol. 62
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6.
Tetrasomy 8 as a primary chromosomal abnormality in a child with acute megakaryoblastic leukemia. a case report and review of the literature.
[electronic resource]
by
Aktas, D
Tuncbilek, E
Cetin, M
Hicsonmez, G
Producer:
20010621
In:
Cancer genetics and cytogenetics
vol. 126
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7.
Butylcyanoacrylate tissue adhesive for columellar incision closure.
[electronic resource]
by
Ozturan, O
Miman, M C
Aktas, D
Oncel, S
Producer:
20010830
In:
The Journal of laryngology and otology
vol. 115
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8.
No evidence for overexpression of the p53 protein and mutations in exons 4-9 of the p53 gene in a large family with adenomatous polyposis.
[electronic resource]
by
Aktas, D
Ayhan, A
Tunçbilek, E
Ozdemir, A
Uzunalimoğlu, B
Producer:
19980915
In:
The American journal of gastroenterology
vol. 93
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9.
Myelodysplastic syndrome associated with monosomy 7 in a child with Bloom syndrome.
[electronic resource]
by
Aktas, D
Koc, A
Boduroglu, K
Hicsonmez, G
Tuncbilek, E
Producer:
20000113
In:
Cancer genetics and cytogenetics
vol. 116
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10.
Undifferentiated carcinoma with lymphoid stroma of the parotid gland.
[electronic resource]
by
Dündar, A
Dereköy, S
Onder, T
Aktaş, D
Ozünlü, A
Producer:
19940224
In:
The Journal of laryngology and otology
vol. 107
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11.
Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology.
[electronic resource]
by
Tunçbilek, E
Alikasifoğlu, M
Boduroğlu, K
Aktas, D
Anar, B
Producer:
19990624
In:
American journal of medical genetics
vol. 84
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12.
Oral lichen planus: an unusual cause of facial and abducens nerve paralysis associated with conjunctival and oesophageal involvement.
[electronic resource]
by
Tunca, A
Calikoglu, E
Aktaş, D
Safak, N
Ustün, H
Producer:
20050107
In:
Journal of the European Academy of Dermatology and Venereology : JEADV
vol. 18
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13.
CYP1A1 gene polymorphism and risk of endometrial hyperplasia and endometrial carcinoma.
[electronic resource]
by
Esinler, I
Aktas, D
Alikasifoglu, M
Tuncbilek, E
Ayhan, A
Producer:
20070227
In:
International journal of gynecological cancer : official journal of the International Gynecological Cancer Society
vol. 16
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14.
Type 1 sirenomelia in one of male twins, with imperforate anus in the other male twin.
[electronic resource]
by
Akbiyik, F
Balci, S
Akkoyun, I
Aktaş, D
Cakmak, O
Producer:
20001207
In:
Clinical dysmorphology
vol. 9
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15.
Coexistent mosaic monosomy 21 and fragile X syndrome in a mentally retarded male patient.
[electronic resource]
by
Utine, G E
Aktas, D
Boduroğlu, K
Alikasifoğlu, M
Tunçbilek, E
Producer:
20071016
In:
Genetic counseling (Geneva, Switzerland)
vol. 18
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16.
TWO CASES WITH DIFFERENT EPILEPSY TYPE AND DYSMORPHIC FEATURES ASSOCIATED WITH 17q21.31 MICRODELETION SYNDROME.
[electronic resource]
by
Uctepe, E
Aktas, D
Alikasifoglu, M
Gunduz, E
Sonmez, F M
Producer:
20181016
In:
Genetic counseling (Geneva, Switzerland)
vol. 27
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17.
Glutathione S-transferase M1 gene polymorphism in bladder cancer patients. a marker for invasive bladder cancer?
[electronic resource]
by
Aktas, D
Ozen, H
Atsu, N
Tekin, A
Sozen, S
Tuncbilek, E
Producer:
20010426
In:
Cancer genetics and cytogenetics
vol. 125
Online resources:
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18.
Antrochoanal polyps: analysis of 16 cases.
[electronic resource]
by
Aktaş, D
Yetişer, S
Gerek, M
Kurnaz, A
Can, C
Kahramanyol, M
Producer:
19981210
In:
Rhinology
vol. 36
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19.
Diploid-triploid and tetraploid mosaicism in a child with cryptogenic cirrhosis and membranous glomerulonephritis: a causal relationship or coincidental association?
[electronic resource]
by
Topaloğlu, R
Aktaş, D
Bakkaloğlu, A
Balci, S
Doğru, D
Oztürk, R
Producer:
19980824
In:
The Turkish journal of pediatrics
vol. 40
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20.
31 cases with oculoauriculovertebral dysplasia (Goldenhar syndrome): clinical, neuroradiologic, audiologic and cytogenetic findings.
[electronic resource]
by
Engiz, O
Balci, S
Unsal, M
Ozer, S
Oguz, K K
Aktas, D
Producer:
20080312
In:
Genetic counseling (Geneva, Switzerland)
vol. 18
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