A plea to search for deletion polymorphism through genome scans in populations

Trends in Genetics

Volumn 16, Issue 10, 2000, Pages 435-437

  Siniscalco, Marcello ^a   Robledo, Renato ^a   Orru, Sandro ^b   Contu, Licinio ^b   Yadav, Prem ^c   Ren, Qun ^d   Lai, Hongshing ^d   Roe, Bruce ^d  

^a Laboratory of Molecular and Cellular Biology of Hematopoiesis   (United States)

^b UNIVERSITY OF CAGLIARI   (Italy)

^c University of Medicine and Dentistry   (United States)

^d UNIVERSITY OF OKLAHOMA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA FRAGMENT;

CHROMOSOME 22; DNA SEQUENCE; GENE DELETION; GENETIC POLYMORPHISM; GENOME; HUMAN; MEDICAL GENETICS; PHENOTYPE; POPULATION GENETICS; PRIORITY JOURNAL; SHORT SURVEY;

EID: 0034307480     PISSN: 01689525     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-9525(00)02101-6     Document Type: Letter

References (11)

1. The DNA sequence of human chromosome 22
2. Cloning the difference between two complex genomes
3. Comparative genomic analysis of tumors: detection of DNA losses and amplification
4. One megabase sequence analysis of the human immunoglobulin λ gene locus
5. Vλ and Jλ-Cλ gene segments of the human immunoglobulin λ light chain locus are separated by 14 kb and rearranged by a deletion mechanism
6. Medical implications of HGP's sequence of chromosome 22
7. A common molecular basis for rearrangement disorders on chromosome 22q11
8. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis
9. Gaps in the human genome project
10. On the strategies and priorities for sequencing the human genome: a personal view
11. High density synthetic oligonucleotide arrays