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مکتبة رقمیه للعلوم الطبيه
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Results of search for 'au:"Altunoglu, U"'
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Authors
Aghayev, A
Altunoglu, U
Avci, S
Bagirova, G
Basaran, S
Deymeer, F
Durmus, H
Karaman, B
Kayserili, H
Kayserili, Hülya
Oflazer-Serdaroglu, P
Ozgur, H
Parman, Y
Sevinc Rustemoglu, B
Tekturk, P
Toksoy, G
Topaloglu, H
Uyguner, Z O
Yapici, Z
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Cohort Studies
Consanguinity
DNA-Binding Proteins
Dystrophin
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High-Throughput Nucleotide Sequencing
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Your search returned 2 results.
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1.
Mild nasal malformations and parietal foramina caused by homozygous ALX4 mutations.
[electronic resource]
by
Kayserili, Hülya
Altunoglu, U
Ozgur, H
Basaran, S
Uyguner, Z O
Producer:
20130620
In:
American journal of medical genetics. Part A
vol. 158A
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2.
Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counseling.
[electronic resource]
by
Toksoy, G
Durmus, H
Aghayev, A
Bagirova, G
Sevinc Rustemoglu, B
Basaran, S
Avci, S
Karaman, B
Parman, Y
Altunoglu, U
Yapici, Z
Tekturk, P
Deymeer, F
Topaloglu, H
Kayserili, H
Oflazer-Serdaroglu, P
Uyguner, Z O
Producer:
20200824
In:
Neuromuscular disorders : NMD
vol. 29
Online resources:
Available from publisher's website
Availability:
No items available.
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