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

Joenje, H; Lo ten Foe, J R; Oostra, A B; van Berkel, C G; Rooimans, M A; Schroeder-Kurth, T; Wegner, R D; Gille, J J; Buchwald, M; Arwert, F

Joenje, H; Lo ten Foe, J R; Oostra, A B; van Berkel, C G; Rooimans, M A; Schroeder-Kurth, T; Wegner, R D; Gille, J J; Buchwald, M; Arwert, F.

Affiliation

Joenje H; Department of Human Genetics, Free University, Amsterdam, The Netherlands.

Blood ; 86(6): 2156-60, 1995 Sep 15.

Article in En | MEDLINE | ID: mdl-7662964

Subject(s)

Fanconi Anemia/classification; Cell Fusion; Cell Line; Chromosome Aberrations; Fanconi Anemia/genetics; Fanconi Anemia/pathology; Genes, Recessive; Genetic Complementation Test; Humans; Infant, Newborn; Lymphocytes/ultrastructure; Male

Search on Google

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Fanconi Anemia Limits: Humans / Male / Newborn Language: En Journal: Blood Year: 1995 Type: Article Affiliation country: Netherlands

Search on Google

XML

PubMed Links