Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome
- 1 March 1994
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 93 (3) , 248-254
- https://doi.org/10.1007/bf00212017
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Deletion Mapping of Chromosome 1p and 22q in PheochromocytomaJapanese Journal of Cancer Research, 1993
- A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locusGenomics, 1992
- Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22Genomics, 1991
- 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
- Toward a long-range map of human chromosomal band 22q11Genomics, 1989
- A genetic linkage map of the long arm of human chromosome 22Genomics, 1989
- Interstitial deletion of chromosome 22 in a patient with the DiGeorge malformation sequenceAmerican Journal of Medical Genetics, 1989
- Loss of constitutional heterozygosity in colon carcinoma from patients with familial polyposis coliNature, 1988
- Characterization of the Philadelphia chromosome by gene mappingCytogenetic and Genome Research, 1981
- Regional localization of the genes coding for human ACO2, ARSA, and NAGA on chromosome 22Cytogenetic and Genome Research, 1980