Literature DB >> 3184145

Prenatal diagnosis of mosaicism for del(18)(q12.2q21.1) and a normal cell line.

M G Wilson1, M S Lin.   

Abstract

Mesh：

Year:  1988        PMID： 3184145      PMCID： PMC1051545          DOI： 10.1136/jmg.25.9.635

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  3 in total

1.  [PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18].

Authors:  J DE GROUCHY; P ROYER; C SALMON; M LAMY
Journal:  Pathol Biol       Date:  1964-05

2.  United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis.

Authors:  L Y Hsu; T E Perlis
Journal:  Prenat Diagn       Date:  1984       Impact factor: 3.050

3.  Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].

Authors:  M G Wilson; J W Towner; I Forsman; E Siris
Journal:  Am J Med Genet       Date:  1979
  3 in total
  2 in total

1.  Mosaicism with a normal cell line and an autosomal structural rearrangement.

Authors:  R J Gardner; H E Dockery; P H Fitzgerald; R G Parfitt; D R Romain; N Scobie; R L Shaw; P Tumewu; A J Watt
Journal:  J Med Genet       Date:  1994-02       Impact factor: 6.318

Review 2.  Interstitial deletion of the long arm of chromosome 18, del(18)(q12.2q21.1): a report of three cases of an autosomal deletion with a mild phenotype.

Authors:  A Schinzel; F Binkert; D M Lillington; M Sands; R J Stocks; R H Lindenbaum; H Matthews; H Sheridan
Journal:  J Med Genet       Date:  1991-05       Impact factor: 6.318
  2 in total

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