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Novel insight into the phenotype of microcephaly 19 in the patient with missense COPB2 mutation.
Shiri, Amirmasoud; Jafari Khamirani, Hossein; Kamal, Neda; Manoochehri, Jamal; Dianatpour, Mehdi; Tabei, Seyed Mohammad Bagher; Dastgheib, Seyed Alireza.
Affiliation
  • Shiri A; School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Jafari Khamirani H; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Kamal N; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Manoochehri J; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Dianatpour M; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran; Stem Cells Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Tabei SMB; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran; Maternal-fetal Medicine Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Dastgheib SA; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran. Electronic address: dastgheib@sums.ac.ir.
Eur J Med Genet ; 66(10): 104846, 2023 Oct.
Article in En | MEDLINE | ID: mdl-37734708
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2023 Document type: Article Affiliation country: Irán Country of publication: Países Bajos
Fulltext
Add to My VHL
Print
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2023 Document type: Article Affiliation country: Irán Country of publication: Países Bajos