Linkage of Familial Hemophagocytic Lymphohistiocytosis to 10q21-22 and Evidence for Heterogeneity
- 1 January 1999
- journal article
- Published by Elsevier in The American Journal of Human Genetics
- Vol. 64 (1) , 172-179
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Hereditary Geniospasm: Linkage to Chromosome 9q13-q21 and Evidence for Genetic HeterogeneityThe American Journal of Human Genetics, 1997
- Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va geneNature Genetics, 1997
- Identification and mutation analysis of the complete gene for Chediak–Higashi syndromeNature Genetics, 1996
- A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 1996
- Genomic organization and chromosomal location of the human gene encoding the B-lymphocyte activation antigen B7Immunogenetics, 1992
- Incidence in Sweden and Clinical Features of Familial Hemophagocytic LymphohistiocytosisActa Paediatrica, 1991
- HISTIOCYTOSIS SYNDROMES IN CHILDRENThe Lancet, 1987
- Linkage analysis and family classification under heterogeneityAnnals of Human Genetics, 1983
- X-LINKED RECESSIVE PROGRESSIVE COMBINED VARIABLE IMMUNODEFICIENCY (DUNCAN'S DISEASE)The Lancet, 1975
- Familial Haemophagocytic ReticulosisArchives of Disease in Childhood, 1952