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Genetic Diagnosis of Children With Neurodevelopmental Disorders Using Whole Genome Sequencing.
Shin, Sunghwan; Lee, Jiwon; Kim, Young-Gon; Ha, Changhee; Park, Jong-Ho; Kim, Jong-Won; Lee, Jeehun; Jang, Ja-Hyun.
Affiliation
  • Shin S; Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea; Department of Laboratory Medicine, Inje University Ilsan Paik Hospital, Goyang, Korea.
  • Lee J; Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Kim YG; Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Ha C; Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Park JH; Clinical Genomics Center, Samsung Medical Center, Seoul, Korea.
  • Kim JW; Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Lee J; Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Jang JH; Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. Electronic address: jahyun.jang@gmail.com.
Pediatr Neurol ; 149: 44-52, 2023 Dec.
Article de En | MEDLINE | ID: mdl-37776660
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Variations de nombre de copies de segment d'ADN / Troubles du développement neurologique Type d'étude: Diagnostic_studies / Guideline Limites: Child / Humans Langue: En Journal: Pediatr Neurol Sujet du journal: NEUROLOGIA / PEDIATRIA Année: 2023 Type de document: Article Pays de publication: États-Unis d'Amérique
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Variations de nombre de copies de segment d'ADN / Troubles du développement neurologique Type d'étude: Diagnostic_studies / Guideline Limites: Child / Humans Langue: En Journal: Pediatr Neurol Sujet du journal: NEUROLOGIA / PEDIATRIA Année: 2023 Type de document: Article Pays de publication: États-Unis d'Amérique