A prenatal diagnosis case of partial duplication 21q21.1-q21.2 with normal phenotype maternally inherited.

Jin, Chunyan; Gu, Zhiping; Jiang, Xiaohan; Yu, Pei; Xu, Tianhui

Jin, Chunyan; Gu, Zhiping; Jiang, Xiaohan; Yu, Pei; Xu, Tianhui.

Afiliación

Jin C; Department of Medical Genetics and Prenatal Diagnosis, Hospital Affiliated 5 to Nantong University (Taizhou People's Hospital), 399 Hailing South Road, Taizhou, 225300, Jiangsu, China.
Gu Z; Department of Medical Genetics and Prenatal Diagnosis, Hospital Affiliated 5 to Nantong University (Taizhou People's Hospital), 399 Hailing South Road, Taizhou, 225300, Jiangsu, China.
Jiang X; Department of Medical Genetics and Prenatal Diagnosis, Hospital Affiliated 5 to Nantong University (Taizhou People's Hospital), 399 Hailing South Road, Taizhou, 225300, Jiangsu, China.
Yu P; Department of Medical Genetics and Prenatal Diagnosis, Hospital Affiliated 5 to Nantong University (Taizhou People's Hospital), 399 Hailing South Road, Taizhou, 225300, Jiangsu, China.
Xu T; Department of Medical Genetics and Prenatal Diagnosis, Hospital Affiliated 5 to Nantong University (Taizhou People's Hospital), 399 Hailing South Road, Taizhou, 225300, Jiangsu, China. xth19921008@163.com.

BMC Med Genomics ; 14(1): 164, 2021 06 19.

Article en En | MEDLINE | ID: mdl-34147104

Asunto(s)

Herencia Materna

Palabras clave

Down syndrome; Down syndrome critical region (DSCR); Partial duplication 21; Prenatal diagnosis

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Herencia Materna Tipo de estudio: Diagnostic_studies Idioma: En Revista: BMC Med Genomics Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google