Your browser doesn't support javascript.
loading
[Primary ciliary dyskinesia caused by mutation of CCNO29 gene in a family report].
Sun, X P; Xu, J X; Wu, S Z; Zhu, H Y; Liu, H; Liu, Z Y; Yang, S; Lu, C Y; Chen, D H.
Affiliation
  • Sun XP; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
  • Xu JX; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
  • Wu SZ; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
  • Zhu HY; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
  • Liu H; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
  • Liu ZY; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
  • Yang S; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
  • Lu CY; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
  • Chen DH; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Zhonghua Er Ke Za Zhi ; 62(4): 378-380, 2024 Mar 25.
Article in Zh | MEDLINE | ID: mdl-38527512
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kartagener Syndrome Limits: Humans Language: Zh Journal: Zhonghua Er Ke Za Zhi Year: 2024 Document type: Article Affiliation country: China
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kartagener Syndrome Limits: Humans Language: Zh Journal: Zhonghua Er Ke Za Zhi Year: 2024 Document type: Article Affiliation country: China