Literature DB >> 1774071

A map of 22 loci on human chromosome 22.

J P Dumanski1, E Carlbom, V P Collins, M Nordenskjöld, B S Emanuel, M L Budarf, H E McDermid, R Wolff, P O'Connell, R White.   

Abstract

We constructed a genetic linkage map of the entire long arm of human chromosome 22 with 30 polymorphic markers, defining 22 loci. The map consists of a continuous linkage group 110 cM long, when male and female recombination fractions are combined; average distance between the loci is 5.2 cM. All loci were placed on the map with high support against alternative orders (odds in excess of 1000:1). The order of loci presented in our map is in full agreement with that of the previous linkage maps of chromosome 22 and with the physical assignment of markers. Two markers included in this map, KI-831 (D22S212) and pEFZ31 (D22S32), allowed us to better define the region of the (11;22) translocation breakpoint specific for Ewing sarcoma. Ten additional polymorphic markers were placed on the 22-loci map with odds lower than 1000:1 against alternative locations. In total, we have introduced 29 new markers on the linkage map of chromosome 22.

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Year:  1991        PMID: 1774071     DOI: 10.1016/0888-7543(91)90079-t

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


  8 in total

1.  Cryptic terminal rearrangement of chromosome 22q13.32 detected by FISH in two unrelated patients.

Authors:  K F Doheny; H E McDermid; K Harum; G H Thomas; G V Raymond
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

2.  Genetic mapping of 14 short tandem repeat polymorphisms on human chromosome 22.

Authors:  H P Vallada; J E Collins; I Dunham; E Dawson; R M Murray; M Gill; D A Collier
Journal:  Hum Genet       Date:  1994-06       Impact factor: 4.132

3.  Molecular characterization of a 130-kb terminal microdeletion at 22q in a child with mild mental retardation.

Authors:  A C Wong; Y Ning; J Flint; K Clark; J P Dumanski; D H Ledbetter; H E McDermid
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

4.  Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.

Authors:  A J Dawson; A J Mears; A E Chudley; T Bech-Hansen; H McDermid
Journal:  J Med Genet       Date:  1996-11       Impact factor: 6.318

5.  Neurofibromatosis type 2 appears to be a genetically homogeneous disease.

Authors:  S A Narod; D M Parry; J Parboosingh; G M Lenoir; M Ruttledge; G Fischer; R Eldridge; R L Martuza; M Frontali; J Haines
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

6.  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

7.  Clinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q13.3.

Authors:  N J Nesslinger; J L Gorski; T W Kurczynski; S K Shapira; J Siegel-Bartelt; J P Dumanski; R F Cullen; B N French; H E McDermid
Journal:  Am J Hum Genet       Date:  1994-03       Impact factor: 11.025

8.  A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritance.

Authors:  H Coon; S Jensen; M Hoff; J Holik; R Plaetke; F Reimherr; P Wender; M Leppert; W Byerley
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

  8 in total

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