Skip to content
  • Home
  • Book Bag: 0 items (Full)
    • English
    • 日本語
    • 中文(简体)
    • 中文(繁體)
    • اللغة العربية
  • About
Advanced
  • P806: Application value of non...
  • Cite this
  • Text this
  • Print
  • Export Record
    • Export to RefWorks
    • Export to EndNoteWeb
    • Export to EndNote
  • Add to Book Bag Remove from Book Bag
  • Permanent link

P806: Application value of noninvasive prenatal diagnosis of recessive monogenic genetic diseases based on relative haplotype dosage changes

Bibliographic Details
Published in:Genetics in Medicine Open
Main Authors: Huanyun Li, Xinyu Fu, Jingqi Zhu, Xiangdong Kong
Format: Article
Language:English
Published: Elsevier 2025-01-01
Online Access:http://www.sciencedirect.com/science/article/pii/S2949774425012142
  • Holdings
  • Description
  • Similar Items
  • Staff View

Internet

http://www.sciencedirect.com/science/article/pii/S2949774425012142

Similar Items

  • O58: High-resolution haplotyping of PAH gene enables early gestation noninvasive prenatal diagnosis of phenylketonuria and evolution analysis of recurrent pathogenic variations
    by: Jingqi Zhu, et al.
    Published: (2025-01-01)
  • P813: Noninvasive prenatal diagnosis of facioscapulohumeral muscular dystrophy using SNP-based amplicon sequencing
    by: Xinyu Fu, et al.
    Published: (2025-01-01)
  • Noninvasive prenatal diagnosis of β‐thalassemia by relative haplotype dosage without analyzing proband
    by: Haoxian Li, et al.
    Published: (2019-11-01)
  • Prenatal genetic diagnosis of monogenic diseases
    by: Prior-de Castro Carmen, et al.
    Published: (2023-03-01)
  • Noninvasive prenatal diagnosis (NIPD) of non-syndromic hearing loss (NSHL) for singleton and twin pregnancies in the first trimester
    by: Huanyun Li, et al.
    Published: (2025-01-01)

Search Options

  • Search History
  • Advanced Search

Find More

  • Browse the Catalog
  • Browse Alphabetically
  • Explore Channels
  • Course Reserves
  • New Items

Need Help?

  • Search Tips
  • Ask a Librarian
  • FAQs