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The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions.
Eur J Hum Genet. 2016 Oct;24(10):1445-52. doi: 10.1038/ejhg.2016.9. Epub 2016 Mar 9.
Eur J Hum Genet. 2016.
PMID: 26956250
Free PMC article.
The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions.
Reddy R, Nguyen NM, Sarrabay G, Rezaei M, Rivas MC, Kavasoglu A, Berkil H, Elshafey A, Abdalla E, Nunez KP, Dreyfus H, Philippe M, Hadipour Z, Durmaz A, Eaton EE, Schubert B, Ulker V, Hadipour F, Touitou I, Fardaei M, Slim R.
Reddy R, et al. Among authors: kavasoglu a.
Eur J Hum Genet. 2016 Oct;24(10):1516. doi: 10.1038/ejhg.2016.96.
Eur J Hum Genet. 2016.
PMID: 27628567
Free PMC article.
No abstract available.
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Mutation analysis of the NRXN1 gene in autism spectrum disorders.
Onay H, Kacamak D, Kavasoglu AN, Akgun B, Yalcinli M, Kose S, Ozbaran B.
Onay H, et al. Among authors: kavasoglu an.
Balkan J Med Genet. 2017 Mar 8;19(2):17-22. doi: 10.1515/bjmg-2016-0031. eCollection 2016 Dec 1.
Balkan J Med Genet. 2017.
PMID: 28289584
Free PMC article.
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[The Role of Molecular Karyotyping in the Genetic Etiology of Autism].
Özbaran B, Akgün B, Kaçamak D, Köse S, Kavasoğlu A, Onay H.
Özbaran B, et al. Among authors: kavasoglu a.
Turk Psikiyatri Derg. 2017 Fall;28(3):156-162.
Turk Psikiyatri Derg. 2017.
PMID: 28936814
Free article.
Turkish.
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