Refinement of the chromosome 5p locus for craniometaphyseal dysplasia

Human Genetics

Volumn 108, Issue 5, 2001, Pages 394-397

  Chandler, D ^a   Tinschert, S ^a   Lohan, K ^a   Harrop, K ^a   Goldblatt, J ^a   Nagy, M ^a   Hummel, S ^a   Braun, H S ^a   Laing, N ^a   Nurnberg P ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BONE DYSPLASIA; BONE METABOLISM; CHROMOSOME 5; CHROMOSOME MARKER; DISEASE CLASSIFICATION; FAMILIAL INCIDENCE; FEMALE; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; GENETIC RECOMBINATION; HAPLOTYPE; HUMAN; HYPEROSTOSIS; MALE; METAPHYSIS; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SCLEROSIS; SKULL DISEASE;

AUSTRALIA; BONE DISEASES, DEVELOPMENTAL; CHROMOSOMES, HUMAN, PAIR 5; FEMALE; GENES, DOMINANT; GENETIC MARKERS; GERMANY; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; PEDIGREE; RECOMBINATION, GENETIC; REPRODUCIBILITY OF RESULTS;

EID: 17844399541     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390100515     Document Type: Article

References (8)

1. Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition disease
2. Faster sequential genetic linkage computations
3. A comprehensive genetic map of the human genome based on 5,264 microsatellites
4. Isolation and characterization of DNA from archaeological bone
5. The gene for autosomal dominant craniometaphyseal dysplasia maps to chromosome 5p and is distinct from the growth hormone-receptor gene
6. Die kraniometaphysäre dysplasie (pyle)
7. Dominant craniometaphyseal dysplasia - A family study over five generations
8. Craniometaphyseal dysplasia in six generations of a German kindred