Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22
Open Access
- 31 August 1991
- Vol. 10 (4), 996-1002
- https://doi.org/10.1016/0888-7543(91)90190-p
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndromeGenomics, 1990
- Monosomy 22 in Rhabdoid or Atypical Teratoid Tumors of the BrainNew England Journal of Medicine, 1989
- Characterization of the Supernumerary Chromosome in Cat Eye SyndromeScience, 1986
- Separation of chromosomal DNA molecules from yeast by orthogonal-field-alternation gel electrophoresisNucleic Acids Research, 1984
- The association of the DiGeorge anomalad with partial monosomy of chromosome 22The Journal of Pediatrics, 1982
- A deletion in chromosome 22 can cause digeorge syndromeHuman Genetics, 1981
- The 11q;22q translocation: A European collaborative analysis of 43 casesHuman Genetics, 1980
- A new translocation in Burkitt's tumor cellsHuman Genetics, 1979
- The Philadelphia Chromosome (Ph1) in Adults Presenting with Acute Leukaemia: a Comparison of Ph1+ and Ph1‐ Patients*British Journal of Haematology, 1977
- Screening λgt Recombinant Clones by Hybridization to Single Plaques in SituScience, 1977