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A report on seven fetal cases associated with 15q11-q13 microdeletion and microduplication.
Huang, Xiuzhu; Chen, Jieping; Hu, Wenlong; Li, Lu; He, Huiyan; Guo, Hui; Liao, Qiuyan; Ye, Mei; Tang, Donge; Dai, Yong.
Afiliação
  • Huang X; MOE Key Laboratory of Tumor Molecular Biology and Key Laboratory of Functional Protein Research of Guangdong Higher Education Institutes, Institute of Life and Health Engineering, College of Life Science and Technology, Jinan University, Guangzhou, China.
  • Chen J; Clinical Medical Research Center, The Second Clinical Medical College of Jinan University (Shenzhen People's Hospital), Shenzhen, China.
  • Hu W; Clinical Medical Research Center, The Second Clinical Medical College of Jinan University (Shenzhen People's Hospital), Shenzhen, China.
  • Li L; Clinical Medical Research Center, The Second Clinical Medical College of Jinan University (Shenzhen People's Hospital), Shenzhen, China.
  • He H; MOE Key Laboratory of Tumor Molecular Biology and Key Laboratory of Functional Protein Research of Guangdong Higher Education Institutes, Institute of Life and Health Engineering, College of Life Science and Technology, Jinan University, Guangzhou, China.
  • Guo H; Clinical Medical Research Center, The Second Clinical Medical College of Jinan University (Shenzhen People's Hospital), Shenzhen, China.
  • Liao Q; Clinical Medical Research Center, The Second Clinical Medical College of Jinan University (Shenzhen People's Hospital), Shenzhen, China.
  • Ye M; Clinical Medical Research Center, The Second Clinical Medical College of Jinan University (Shenzhen People's Hospital), Shenzhen, China.
  • Tang D; Clinical Medical Research Center, The Second Clinical Medical College of Jinan University (Shenzhen People's Hospital), Shenzhen, China.
  • Dai Y; Clinical Medical Research Center, The Second Clinical Medical College of Jinan University (Shenzhen People's Hospital), Shenzhen, China.
Mol Genet Genomic Med ; 9(3): e1605, 2021 03.
Article em En | MEDLINE | ID: mdl-33538077
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Feto / Deficiência Intelectual Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Feto / Deficiência Intelectual Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China