Assignment of ferritin L gene (FTL) to human chromosome band 19q13.3 by in situ hybridization

Annales de Genetique

Volumn 40, Issue 4, 1997, Pages 227-228

  Gasparini, P ^a   Calvano, S ^a   Memeo, E ^a   Bisceglia, L ^a   Zelante, L ^a  

^a IRCCS Ospedale 'CSS'   (Italy)

Author keywords

FISH localisation; FTL gene

Indexed keywords

FERRITIN;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 19Q; CONGENITAL CATARACT; FERRITIN BLOOD LEVEL; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; HYBRID CELL; HYPERFERRITINEMIA;

APOFERRITINS; CATARACT; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 19; FERRITINS; GENES, DOMINANT; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; SYNDROME;

EID: 0031439894     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)