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Dergiler / Balkan Medical Journal / 2020 / Cilt: 37 - Sayı: 5

Two Cases of Cystic Fibrosis with Compound Heterozygous Variants Reported for the First Time

Sinem YALÇINTEPE
Hakan GÜRKAN
Ümit Nusret BAŞARAN
Niyazi Cenk SAYIN
Engin ATLI
Sayfa
297–298
Yayın Tarihi
2022-10-11
DOI
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YALÇINTEPE, S., GÜRKAN, H., BAŞARAN, Ü. N., SAYIN, N. C., ATLI, E. (2022). Two Cases of Cystic Fibrosis with Compound Heterozygous Variants Reported for the First Time. Balkan Medical Journal, Cilt: 37 - Sayı: 5, 297–298. https://ajindex.com/articles/460907

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Kaynakça (4)

  1. Sharma N, Cutting GR. The genetics and genomics of cystic fibrosis. J Cyst Fibros 2020;19(Suppl 1):5-9
  2. Paranjapye A, Ruffin M, Harris A, Corvol H. Genetic variation in CFTR and modifier loci may modulate cystic fibrosis disease severity. J Cyst Fibros 2020;19(Suppl 1):10- 4
  3. Sugunaraj JP, Brosius HM, Murray MF, Manickam K, Stamm JA, Carey DJ, et al. Predictive value of genomic screening: cross-sectional study of cystic fibrosis in 50,788 electronic health records. NPJ Genom Med 2019;4:21
  4. Hangül M, Pekcan S, Köse M, Acıcan D, Şahlar TE, Erdoğan M, et al. The Incidence of Cystic Fibrosis in the Central Region of Anatolia in Turkey Between 2015 and 2016. Balkan Med J 2019;36:179-83.