Literature DB >> 8222751

Report and abstracts of the second international workshop on human chromosome 18 mapping. Doorwerth, the Netherlands, July 19-20, 1993.

A G van Kessel1, R E Straub, G A Silverman, S Gerken, J Overhauser.   

Abstract

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Year:  1994        PMID： 8222751

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


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  10 in total

1.  Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakers.

Authors:  M Starfield; H C Hennies; M Jung; T Jenkins; T Wienker; P Hull; A Spurdle; W Küster; M Ramsay; A Reis
Journal:  Am J Hum Genet       Date:  1997-08       Impact factor: 11.025

2.  Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing.

Authors:  T Eggermann; H Engels; B Moskalonek; M M Nöthen; J Müller-Navia; E Schleiermacher; G Schwanitz; S Stengel-Rutkowski
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

3.  Comparative mapping in cattle of genes located on human chromosome 18.

Authors:  M K Agaba; S J Kemp; W Barendse; A Teale
Journal:  Mamm Genome       Date:  1997-07       Impact factor: 2.957

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.  cDNA cloning of the rat APC gene and assignment to chromosome 18.

Authors:  M Toyota; T Ushijima; H Kakiuchi; M Watanabe; K Imai; A Yachi; T Sugimura; M Nagao
Journal:  Mamm Genome       Date:  1995-10       Impact factor: 2.957

6.  Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction.

Authors:  J M Fisher; J F Harvey; N E Morton; P A Jacobs
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025

7.  The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2.

Authors:  G A Silverman; S S Schneider; H F Massa; A Flint; M Lalande; J C Leonard; J Overhauser; G van den Engh; B J Trask
Journal:  Am J Hum Genet       Date:  1995-04       Impact factor: 11.025

8.  Chromosome 18 DNA markers and manic-depressive illness: evidence for a susceptibility gene.

Authors:  W H Berrettini; T N Ferraro; L R Goldin; D E Weeks; S Detera-Wadleigh; J I Nurnberger; E S Gershon
Journal:  Proc Natl Acad Sci U S A       Date:  1994-06-21       Impact factor: 11.205

9.  Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunction.

Authors:  T Eggermann; M M Nöthen; B Eiben; D Hofmann; K Hinkel; R Fimmers; G Schwanitz
Journal:  Hum Genet       Date:  1996-02       Impact factor: 4.132

10.  Physical mapping of the holoprosencephaly critical region in 18p11.3.

Authors:  J Overhauser; H F Mitchell; E H Zackai; D B Tick; K Rojas; M Muenke
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025
  10 in total

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