Literature DB >> 2841760

Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci.

L M Davis1, R Stallard, G H Thomas, P Couillin, C Junien, N J Nowak, T B Shows.   

Abstract

The association of Wilms' tumor with aniridia (the WAGR complex) in children with 11p13 chromosomal abnormalities has been established, but the paucity of molecular probes in 11p13 has hampered identification of the responsible genes. Two new anonymous DNA segments have been identified that map to the WAGR region of 11p13. Both DNA probes identify a cytologically undetectable deletion associated with a balanced chromosome translocation inherited by a patient with familial aniridia, but not Wilms' tumor. The same two DNA segments are also included in the distal p13-p14.1 deletion of another patient, who has aniridia, Wilms' tumor, and hypogonadism, but they are not included in the p12-p13 deletion of a third patient, who does not have aniridia but has had a Wilms' tumor. The discovery of this aniridia deletion and these two DNA segments that physically separate the Wilms' tumor and aniridia loci should facilitate identification of the genes in the WAGR locus, beginning with the aniridia gene.

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Year:  1988        PMID: 2841760     DOI: 10.1126/science.2841760

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  17 in total

Review 1.  Mouse chromosome 2.

Authors:  L D Siracusa; C M Abbott
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

2.  Somatic cell hybrid and long-range physical mapping of 11p13 microdissected genomic clones.

Authors:  L M Davis; G Senger; H J Lüdecke; U Claussen; B Horsthemke; S S Zhang; B Metzroth; K Hohenfellner; B Zabel; T B Shows
Journal:  Proc Natl Acad Sci U S A       Date:  1990-09       Impact factor: 11.205

3.  A deletion map of the WAGR region on chromosome 11.

Authors:  M Gessler; G H Thomas; P Couillin; C Junien; B C McGillivray; M Hayden; G Jaschek; G A Bruns
Journal:  Am J Hum Genet       Date:  1989-04       Impact factor: 11.025

4.  Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

Authors:  R A Lewis
Journal:  Trans Am Ophthalmol Soc       Date:  1989

5.  Isolation and regional localisation of DNA sequences from a human chromosome 11-specific cosmid library.

Authors:  R B Wadey; P F Little; J Pritchard; J K Cowell
Journal:  Hum Genet       Date:  1990-04       Impact factor: 4.132

6.  Molecular cytogenetics: toward dissection of the contiguous gene syndromes.

Authors:  B S Emanuel
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

Review 7.  Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.

Authors:  N Tommerup
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

8.  Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studies.

Authors:  N B Spinner; E B Rand; P Fortina; A Genin; R Taub; A Semeraro; D A Piccoli
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

9.  Insertional inactivation of the WT1 gene in tumour cells from a patient with WAGR syndrome.

Authors:  A Santos; L Osorio-Almeida; P N Baird; J M Silva; M G Boavida; J Cowell
Journal:  Hum Genet       Date:  1993-08       Impact factor: 4.132

10.  Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.

Authors:  D E Merry; J G Lesko; D M Sosnoski; R A Lewis; M Lubinsky; B Trask; G van den Engh; F S Collins; R L Nussbaum
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

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