A novel mechanism for thalassaemia intermedia

Lancet

Volumn 359, Issue 9301, 2002, Pages 132-133

  Badens, C ^a,e   Mattei, M G ^b   Imbert, A M ^c   Lapoumeroulie C ^b   Martini, N ^a   Michel, G ^d   Lena Russo, D ^a  

^a CERGM Laboratoire des Hémoglobines   (France)

^b INSERM   (France)

^c INSTITUT PAOLI CALMETTES   (France)

^d TIMONE HOSPITAL   (France)

^e AIX MARSEILLE UNIVERSITY   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BETA GLOBIN;

ARTICLE; BETA THALASSEMIA; GENE DELETION; GENE LOCUS; GENETIC DISORDER; HEMATOPOIETIC SYSTEM; HEMOGLOBIN ANALYSIS; HETEROZYGOSITY; HUMAN; MOSAICISM; PRIORITY JOURNAL;

EID: 0037065526     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(02)07338-5     Document Type: Article

References (5)

1. Relationship between genotype and phenotype: Thalassemia intermedia
2. Delineation of the centromeric and telomeric chromosome segment 11p15,5 lung cancer suppressor regions LOH11A and LOH11B
3. Genetic changes in epithelial solid neoplasia
4. A 1,4 Mb high-resolution physical map and contig of chromosome segment 11p15.5 and genes in the LOH11A metastasis suppressor region
5. Nontransfusional iron overload in thalassemia: Association with hereditary hemochromatosis