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Clinical application of single-molecule optical mapping to a multigeneration FSHD1 pedigree.
Zhang, Qian; Xu, Xueqin; Ding, Lirong; Li, Huanzheng; Xu, Chengyang; Gong, Yuyan; Liu, Ying; Mu, Ting; Leigh, Don; Cram, David S; Tang, Shaohua.
Affiliation
  • Zhang Q; Zhejiang Provincial Key Laboratory of Medical Genetics, School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, China.
  • Xu X; Wenzhou Key Laboratory of Birth Defects, Wenzhou Central Hospital, Wenzhou, China.
  • Ding L; Zhejiang Provincial Key Laboratory of Medical Genetics, School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, China.
  • Li H; Wenzhou Key Laboratory of Birth Defects, Wenzhou Central Hospital, Wenzhou, China.
  • Xu C; Wenzhou Key Laboratory of Birth Defects, Wenzhou Central Hospital, Wenzhou, China.
  • Gong Y; Berry Genomics Corporation, Beijing, China.
  • Liu Y; Berry Genomics Corporation, Beijing, China.
  • Mu T; Berry Genomics Corporation, Beijing, China.
  • Leigh D; The First Hospital of Kunming, Kunming, China.
  • Cram DS; Berry Genomics Corporation, Beijing, China.
  • Tang S; Zhejiang Provincial Key Laboratory of Medical Genetics, School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, China.
Mol Genet Genomic Med ; 7(3): e565, 2019 03.
Article in En | MEDLINE | ID: mdl-30666819
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Testing / Muscular Dystrophy, Facioscapulohumeral / Optical Restriction Mapping / Mutation Type of study: Diagnostic_studies / Evaluation_studies / Prognostic_studies Limits: Humans Language: En Journal: Mol Genet Genomic Med Year: 2019 Type: Article Affiliation country: China
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Testing / Muscular Dystrophy, Facioscapulohumeral / Optical Restriction Mapping / Mutation Type of study: Diagnostic_studies / Evaluation_studies / Prognostic_studies Limits: Humans Language: En Journal: Mol Genet Genomic Med Year: 2019 Type: Article Affiliation country: China