Literature DB >> 1577474

Somatic cell hybrid deletion map of human chromosome 18.

A D Kline1, K Rojas, R Mewar, D Moshinsky, J Overhauser.   

Abstract

The creation of a physical map of chromosome 18 will be useful for the eventual identification of specific chromosomal regions that are critical in the occurrence of Edwards syndrome, the 18q- syndrome, and the 18p- syndrome. To begin the investigation of these syndromes, a physical map has been constructed to order random DNA fragments to specific portions of chromosome 18. A set of somatic cell hybrids that retain deletions or translocations involving chromosome 18 has been isolated and characterized. Over 200 lambda phage from a chromosome 18-specific library have been localized to 11 distinct regions of chromosome 18 using the chromosomal breakpoints present in the somatic cell hybrids.

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Year:  1992        PMID: 1577474     DOI: 10.1016/0888-7543(92)90193-v

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


  12 in total

1.  Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3.

Authors:  L Boghosian-Sell; D E Comings; J Overhauser
Journal:  Am J Hum Genet       Date:  1996-11       Impact factor: 11.025

2.  High affinity YY1 binding motifs: identification of two core types (ACAT and CCAT) and distribution of potential binding sites within the human beta globin cluster.

Authors:  S R Yant; W Zhu; D Millinoff; J L Slightom; M Goodman; D L Gumucio
Journal:  Nucleic Acids Res       Date:  1995-11-11       Impact factor: 16.971

3.  Clinical features and mental development of a child with a prenatally identified 45,XX,der(5)t(5;18) (p15;q11.2),-18 karyotype.

Authors:  R G Hutcheon; A Mallik; M Shaham
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318

4.  Molecular characterization of patients with 18q23 deletions.

Authors:  G Strathdee; R Sutherland; J J Jonsson; R Sataloff; M Kohonen-Corish; D Grady; J Overhauser
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

5.  The human cytochrome b5 gene and two of its pseudogenes are located on chromosomes 18q23, 14q31-32.1 and 20p11.2, respectively.

Authors:  S J Giordano; M Yoo; D C Ward; M Bhatt; J Overhauser; A W Steggles
Journal:  Hum Genet       Date:  1993-12       Impact factor: 4.132

Review 6.  Molecular analysis of the 18q- syndrome--and correlation with phenotype.

Authors:  A D Kline; M E White; R Wapner; K Rojas; L G Biesecker; J Kamholz; E H Zackai; M Muenke; C I Scott; J Overhauser
Journal:  Am J Hum Genet       Date:  1993-05       Impact factor: 11.025

7.  Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18.

Authors:  L Boghosian-Sell; R Mewar; W Harrison; R M Shapiro; E H Zackai; J Carey; L Davis-Keppen; L Hudgins; J Overhauser
Journal:  Am J Hum Genet       Date:  1994-09       Impact factor: 11.025

8.  Identification of Evi-3, a novel common site of retroviral integration in mouse AKXD B-cell lymphomas.

Authors:  M J Justice; H C Morse; N A Jenkins; N G Copeland
Journal:  J Virol       Date:  1994-03       Impact factor: 5.103

9.  Interstitial deletions are not the main mechanism leading to 18q deletions.

Authors:  G Strathdee; W Harrison; H C Riethman; S A Goodart; J Overhauser
Journal:  Am J Hum Genet       Date:  1994-06       Impact factor: 11.025

10.  Ablepharon macrostomia syndrome with associated cutis laxa: possible localization to 18q.

Authors:  J E Pellegrino; R E Schnur; L Boghosian-Sell; G Strathdee; J Overhauser; N B Spinner; T Stump; K Grace; E H Zackai
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

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