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pro vyhledávání: '"Sen-Jing Chen"'
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-9 (2021)
Abstract Background Terminal deletion of chromosome 10p is a rare chromosomal abnormality. We report a neonatal case with a large deletion of 10p15.3p13 diagnosed early because of severe clinical manifestations. Case presentation Our patient presente
Externí odkaz:
https://doaj.org/article/f88647a3fbc045b9ab97c6b8176162cd
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-9 (2021)
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-9 (2021)
BackgroundTerminal deletion of chromosome 10p is a rare chromosomal abnormality. We report a neonatal case with a large deletion of 10p15.3p13 diagnosed early because of severe clinical manifestations.Case presentationOur patient presented with speci