Ö. Alper

发表

Association Between Cystic Fibrosis Severity Markers and CFTR Genotypes in Turkish Children.

Elanur Yilmaz, D. F. Kocacik Uygun, A. Bingöl, 2021, Turkish thoracic journal.

Review of Diabetes Mellitus in Relation to Pancreatic Cancer

Saeyoung Ahn, Özge Alper, Ö. Alper, 2021, Clinical Medical Case Reports and Reviews.

Identification of novel and rare mutations in California Hispanic and African American cystic fibrosis patients

K. Hardy, L. Wong, A. Lieberthal, 2004, Human mutation.

Molecular diagnosis of hematological malignancies by RT-PCR

Lu, N. Yakut, G. Tezcan, 2005 .

Comparison of FSH Receptor Polymorphisms Between Infertile andFertile Women

M. Şımşek, M. Akar, B. Sever, 2014 .

Mutational spectrum of MYO15A: the large N‐terminal extension of myosin XVA is required for hearing

S. Riazuddin, Z. Ahmed, S. Riazuddin, 2007, Human mutation.

Recent Advances in Craniosynostosis.

Elanur Yilmaz, B. Nur, S. Tacoy, 2019, Pediatric neurology.

Copy Number Variation Analysis in Turkish Patients with Congenital Bilateral Absence of Vas Deferens

S. Kahraman, M. Usta, Y. Akın, 2021, Acta Medica Alanya.

Advances in Brief Simultaneous Suppression of Epidermal Growth Factor Receptor and c-erbB2 Reverses Aneuploidy and Malignant Phenotype of a Human Ovarian Carcinoma Cell Line

Z. Szallasi, G. Klus, M. Augustus, 2004 .

Two novel null mutations in a Taiwanese cystic fibrosis patient and a survey of East Asian CFTR mutations

L. Wong, Mei‐Hui Lee, Bao‐Tyan Wang, 2003, American journal of medical genetics. Part A.

Normal sweat chloride test does not rule out cystic fibrosis.

A. Bingöl, A. E. Başaran, Ö. Alper, 2017, The Turkish journal of pediatrics.

1154insTC is not a rare CFTR mutation

G. Hostetter, L. Wong, J. Cook, 2003, American journal of medical genetics. Part A.

Novel and rare CFTR gene mutations in Turkish patients with congenital aplasia of vas deferens

M. Usta, G. Lüleci, Y. Akın, 2014, Andrologia.

Maternal Serum Screening for Downs Syndrome, Open Neural Tube Defects and Trisomy 18

G. Lüleci, T. Özben, S. H. Akbaş, 2001, Clinical chemistry and laboratory medicine.

Mutation Analysis By The Use of Temporal Temperature Gradient Gel Electrophoresis

G. Luleci, L. Wong, Ö. Alper, 2005 .

Detection of CFTR mutations using temporal temperature gradient gel electrophoresis

L. Wong, Ö. Alper, 2004, Electrophoresis.

First prenatal exclusion of cystic fibrosis in East Asia

L. Wong, L. Tsao, Ming Chen, 2007, Pediatrics international : official journal of the Japan Pediatric Society.

Initial regional evaluation of the Cystic Fibrosis Newborn Screening Program: data from the Mediterranean coast of Turkey**

D. F. Kocacik Uygun, A. Bingöl, D. Acıcan, 2019, Turkish journal of medical sciences.