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Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disorders.
Wu, Wenman; Zhou, Xuanyou; Jiang, Zhengwen; Zhang, Dazhi; Yu, Feng; Zhang, Lanlan; Wang, Xuefeng; Chen, Songchang; Xu, Chenming.
Afiliación
  • Wu W; Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.
  • Zhou X; Collaborative Innovation Center of Hematology, Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.
  • Jiang Z; Obstetrics and Gynecology Hospital, Institute of Reproduction and Development, Fudan University, Shanghai, People's Republic of China.
  • Zhang D; International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People's Republic of China.
  • Yu F; Shanghai Key Laboratory of Embryo Original Disorders, Shanghai, People's Republic of China.
  • Zhang L; Genesky Diagnostics (Suzhou) Inc., 218 Xinghu St, Suzhou, Jiangsu, People's Republic of China.
  • Wang X; Genesky Diagnostics (Suzhou) Inc., 218 Xinghu St, Suzhou, Jiangsu, People's Republic of China.
  • Chen S; Genesky Diagnostics (Suzhou) Inc., 218 Xinghu St, Suzhou, Jiangsu, People's Republic of China.
  • Xu C; International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People's Republic of China.
Hum Genomics ; 16(1): 28, 2022 07 27.
Article en En | MEDLINE | ID: mdl-35897115
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Feto Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Hum Genomics Asunto de la revista: GENETICA Año: 2022 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Feto Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Hum Genomics Asunto de la revista: GENETICA Año: 2022 Tipo del documento: Article