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Clinically significant maternal X chromosomal copy number variation detected by noninvasive prenatal test.
Kim, Seung-Chul; Cha, Dong-Hyun; Jeong, Hae-Ryun; Lee, Junnam; Jang, Ja-Hyun; Cho, Eun-Hae.
Affiliation
  • Kim SC; Department of Obstetrics and Gynecology, School of Medicine, Pusan National University, Pusan, South Korea.
  • Cha DH; Department of Obstetrics and Gynecology, CHA Gangnam Medical Center, CHA University, Seoul, South Korea.
  • Jeong HR; Department of Obstetrics and Gynecology, Cheil Women's Hospital, Incheon, South Korea.
  • Lee J; Genome Research Center, GC Genome, Yongin, South Korea.
  • Jang JH; Genome Research Center, GC Genome, Yongin, South Korea.
  • Cho EH; Genome Research Center, GC Genome, Yongin, South Korea.
J Obstet Gynaecol Res ; 45(9): 1925-1928, 2019 Sep.
Article in En | MEDLINE | ID: mdl-31215731
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prenatal Diagnosis / Sex Chromosome Aberrations / Genetic Testing / Chromosomes, Human, X / DNA Copy Number Variations Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Pregnancy Language: En Journal: J Obstet Gynaecol Res Journal subject: GINECOLOGIA / OBSTETRICIA Year: 2019 Type: Article Affiliation country: South Korea
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prenatal Diagnosis / Sex Chromosome Aberrations / Genetic Testing / Chromosomes, Human, X / DNA Copy Number Variations Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Pregnancy Language: En Journal: J Obstet Gynaecol Res Journal subject: GINECOLOGIA / OBSTETRICIA Year: 2019 Type: Article Affiliation country: South Korea