Your browser doesn't support javascript.
loading
An intron c.149-2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype.
Floch, Aline; Vege, Sunitha; Berardi, Philip; Hannon, Judith; Ochoa-Garay, Gorka; Lomas-Francis, Christine; Westhoff, Connie M.
Affiliation
  • Floch A; Immunohematology and Genomics Laboratory, New York Blood Center, New York, New York, USA.
  • Vege S; Etablissement francais du sang Ile-de-France, Creteil, France.
  • Berardi P; INSERM U955 Equipe « Transfusion et maladies du globule rouge ¼, IMRB, Univ Paris Est Creteil, Creteil, France.
  • Hannon J; Immunohematology and Genomics Laboratory, New York Blood Center, New York, New York, USA.
  • Ochoa-Garay G; National Immunohematology Reference Laboratory, Canadian Blood Services, Brampton, Ontario, Canada.
  • Lomas-Francis C; Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.
  • Westhoff CM; Immunohematology and Genomics Laboratory, New York Blood Center, New York, New York, USA.
Transfusion ; 62(2): E14-E16, 2022 02.
Article in En | MEDLINE | ID: mdl-34936100
Subject(s)
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rh-Hr Blood-Group System / Blood Group Antigens Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Transfusion Year: 2022 Document type: Article Affiliation country: United States
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rh-Hr Blood-Group System / Blood Group Antigens Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Transfusion Year: 2022 Document type: Article Affiliation country: United States