Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Munira Bulegenova"'
Publikováno v:
Indian pediatrics. 59(5)
To study the frequency and spectrum of CFTR gene variants in different ethnic groups of Kazakhstan.We reviewed the records of 58 patients with cystic fibrosis. All the patients underwent molecular genetic analysis to reveal genotype-phenotype correla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5f9a4a653debbea5ed2340e6fa307fa
https://pubmed.ncbi.nlm.nih.gov/35273129
https://pubmed.ncbi.nlm.nih.gov/35273129
Autor:
Bulegenova M; Laboratory Department, Scientific Center of Pediatrics and Children Surgery, Almaty, Kazakhstan. Correspondence to: Dr Munira Bulegenova, Laboratory Department, Scientific Center of Pediatrics and Children Surgery, Almaty, Kazakhstan. mbulegenova@yandex.kz., Macek M; National Center for Cystic Fibrosis, Prague, Czech Republic., Libik M; Department of Biology and Medical Genetics, Motol University Hospital, 2nd Faculty of Medicine, Charles University in Prague, Czech Republic., Imangaliyeva A; Department of General Somatic, Scientific Center of Pediatrics and Children Surgery, Almaty, Kazakhstan., Makhneva A; Laboratory Department, Scientific Center of Pediatrics and Children Surgery, Almaty, Kazakhstan.
Publikováno v:
Indian pediatrics [Indian Pediatr] 2022 May 15; Vol. 59 (5), pp. 380-383. Date of Electronic Publication: 2022 Mar 10.