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Chronic granulomatous disease associated with Duchenne muscular dystrophy caused by Xp21.1 contiguous gene deletion syndrome: Case report and literature review.
Bi, Shaohua; Dai, Liying; Jiang, Liangliang; Wang, Lili; Teng, Mia; Liu, Guanghui; Teng, Ru-Jeng.
Affiliation
  • Bi S; Division of Neonatology, Anhui Provincial Children's Hospital, Hefei, Anhui, China.
  • Dai L; Division of Neonatology, Anhui Provincial Children's Hospital, Hefei, Anhui, China.
  • Jiang L; Department of Pediatrics, Anhui Provincial Children's Hospital, Hefei, Anhui, China.
  • Wang L; First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
  • Teng M; Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI, United States.
  • Liu G; Division of Neonatology, Anhui Provincial Children's Hospital, Hefei, Anhui, China.
  • Teng RJ; Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI, United States.
Front Genet ; 13: 970204, 2022.
Article in En | MEDLINE | ID: mdl-36712874
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Front Genet Year: 2022 Document type: Article Affiliation country: Country of publication:
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Front Genet Year: 2022 Document type: Article Affiliation country: Country of publication: