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A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33-34
- Source :
- Human genetics. 121(2)
- Publication Year :
- 2006
-
Abstract
- Ghosal hemato-diaphyseal dysplasia is a rare autosomal recessive disorder characterized by a progressive sclerosing diaphyseal dysplasia and refractory anemia. The pathogenesis and genetic bases of this syndrome remain hitherto unknown. We have performed a genome wide search in two inbred families originating from Algeria and Tunisia. Here, we report on the mapping of a disease gene to chromosome 7q33–34 (Z max = 4.21 at θ = 0 at locus D7S2513) in a 3.4 Mb defined by loci D7S2560 and AC091742. Ongoing studies will hopefully lead to identification of the disease-causing gene.
- Subjects :
- Adult
Male
Tunisia
Locus (genetics)
Biology
Genome
Pathogenesis
Gene mapping
Genetics
medicine
Humans
Genetic Predisposition to Disease
Gene
Genetics (clinical)
Family Health
Genome, Human
Chromosome Mapping
Infant
Osteopetrosis
Camurati-Engelmann Syndrome
medicine.disease
Human genetics
Pedigree
Dysplasia
Algeria
Child, Preschool
Female
Chromosomes, Human, Pair 7
Subjects
Details
- ISSN :
- 03406717
- Volume :
- 121
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Human genetics
- Accession number :
- edsair.doi.dedup.....5d7fb879f2d89298facd7133418b48b0