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Biallelic variants in PAX3 cause Klein syndrome.
Salah, Somaya; Meiner, Vardiella; Abumayaleh, Abdelrazzaq; Asafra, Ali; Al-Sharif, Taher; Al-Fallah, Orwa; Hasasneh, Belal; Zlotogora, Joël.
Affiliation
  • Salah S; Department of Genetics, Hadassah Medical Center and the Hebrew University, Jerusalem, Israel.
  • Meiner V; Genetic Unit, Palestine Red Crescent Society Hospital, Hebron, Palestine.
  • Abumayaleh A; Paediatric Department, Palestine Red Crescent Society Hospital, Hebron, Palestine.
  • Asafra A; Department of Genetics, Hadassah Medical Center and the Hebrew University, Jerusalem, Israel.
  • Al-Sharif T; Paediatric Department, Palestine Red Crescent Society Hospital, Hebron, Palestine.
  • Al-Fallah O; Paediatric Department, Palestine Red Crescent Society Hospital, Hebron, Palestine.
  • Hasasneh B; Paediatric Department, Al Ahli Hospital, Hebron, Palestine.
  • Zlotogora J; Radiology Department, Al Ahli Hospital, Hebron, Palestine.
Clin Genet ; 102(3): 223-227, 2022 09.
Article in En | MEDLINE | ID: mdl-35607853
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Waardenburg Syndrome / PAX3 Transcription Factor Type of study: Diagnostic_studies Limits: Child / Humans Language: En Journal: Clin Genet Year: 2022 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Waardenburg Syndrome / PAX3 Transcription Factor Type of study: Diagnostic_studies Limits: Child / Humans Language: En Journal: Clin Genet Year: 2022 Document type: Article Affiliation country: Country of publication: