Literature DB >> 1680800

Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22.

M L Budarf1, H E McDermid, B Sellinger, B S Emanuel.   

Abstract

Thirty-five new, unique, DNA probes have been isolated and each has been assigned to one of five regions on chromosome 22. The distribution of probes along the chromosome is what would be expected based on the estimated size of each region with the exception of the short arm (22p). RFLP analysis was performed using 13 different restriction enzymes and over 50% of the probes were found to have useful polymorphisms. Probes mapping to 22q11 were further characterized by pulsed-field gel analysis and it has been possible to link several on large restriction fragments. These 35 new probes will be useful reagents for producing genetic and physical maps of chromosome 22.

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Year:  1991        PMID: 1680800     DOI: 10.1016/0888-7543(91)90190-p

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  14 in total

1.  A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

Authors:  D A Driscoll; M L Budarf; B S Emanuel
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

Review 2.  Anorectal malformation: the etiological factors.

Authors:  Chen Wang; Long Li; Wei Cheng
Journal:  Pediatr Surg Int       Date:  2015-04-22       Impact factor: 1.827

3.  Mapping of the human lambda immunoglobulin variable gene subgroup 1.

Authors:  H E McDermid; B S Emanuel
Journal:  Immunogenetics       Date:  1994       Impact factor: 2.846

4.  The phenotypic effects of chromosome rearrangement involving bands 7q21.3 and 22q13.3.

Authors:  A Slavotinek; E Maher; P Gregory; P Rowlandson; S M Huson
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318

5.  Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome.

Authors:  B Morrow; R Goldberg; C Carlson; R Das Gupta; H Sirotkin; J Collins; I Dunham; H O'Donnell; P Scambler; R Shprintzen
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

6.  Metachromatic leucodystrophy (MLD) in a patient with a constitutional ring chromosome 22.

Authors:  M B Coulter-Mackie; J Rip; M D Ludman; J Beis; D E Cole
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

7.  Molecular characterization of the marker chromosome associated with cat eye syndrome.

Authors:  A J Mears; A M Duncan; M L Budarf; B S Emanuel; B Sellinger; J Siegel-Bartelt; C R Greenberg; H E McDermid
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

8.  Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region.

Authors:  A J Mears; H el-Shanti; J C Murray; H E McDermid; S R Patil
Journal:  Am J Hum Genet       Date:  1995-09       Impact factor: 11.025

9.  Analysis of chromosome 22 deletions in neurofibromatosis type 2-related tumors.

Authors:  R K Wolff; K A Frazer; R K Jackler; M J Lanser; L H Pitts; D R Cox
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

10.  Use of fluorescence in situ hybridization (FISH) in the diagnosis of DiGeorge sequence and related diseases.

Authors:  R S Larson; M G Butler
Journal:  Diagn Mol Pathol       Date:  1995-12
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