Classification of Fanconi anemia patients by complementation analysis: Evidence for a fifth genetic subtype

Blood

Volumn 86, Issue 6, 1995, Pages 2156-2160

  Joenje, Hans ^a   Lo Ten Foe, Jerome R ^b   Oostra, Anneke B ^b   Van Berkel, Carola G M ^b   Rooimans, Martin A ^b   Schroeder Kurth, Traute ^b   Wegner, Rolf Dieter ^b   Gille, Johan J P ^b   Buchwald, Manuel ^b   Arwert, Fré ^b  

^a VU UNIVERSITY AMSTERDAM   (Netherlands)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BONE MARROW DEPRESSION; CASE REPORT; CELL FUSION; CHILD; FANCONI ANEMIA; GENETIC COMPLEMENTATION; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL; MALE; MARKER GENE; PRESCHOOL CHILD; PRIORITY JOURNAL;

EID: 0029163523     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v86.6.2156.bloodjournal8662156     Document Type: Article

References (13)

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