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Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing PBX1 gene.
Luo, Man; Gu, Xia; Zhou, Ting; Chen, Chaoli.
Affiliation
  • Luo M; Department of Obstetrics, Maternal and Child Health Hospital of Hubei Province, Wuhan, Hubei, People's Republic of China.
  • Gu X; Department of Obstetrics, Maternal and Child Health Hospital of Hubei Province, Wuhan, Hubei, People's Republic of China.
  • Zhou T; Medical Genetics Center, Maternal and Child Health Hospital of Hubei Province, Wuhan, Hubei, People's Republic of China.
  • Chen C; Department of Obstetrics, Maternal and Child Health Hospital of Hubei Province, Wuhan, Hubei, People's Republic of China. lifenhuangshi@126.com.
Mol Cytogenet ; 15(1): 53, 2022 Dec 21.
Article in En | MEDLINE | ID: mdl-36544198
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Mol Cytogenet Year: 2022 Document type: Article Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Mol Cytogenet Year: 2022 Document type: Article Country of publication: