Literature DB >> 2002489

Cornelia de Lange syndrome with ring chromosome 3.

G N Wilson.   

Abstract

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Year:  1991        PMID： 2002489      PMCID： PMC1016788          DOI： 10.1136/jmg.28.2.143

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


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  7 in total

Review 1.  Genomic imprinting: review and relevance to human diseases.

Authors:  J G Hall
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

2.  Cornelia de Lange syndrome with ring chromosome 3.

Authors:  P Lakshminarayana; P Nallasivam
Journal:  J Med Genet       Date:  1990-06       Impact factor: 6.318

3.  Familial de Lange syndrome with chromosome abnormalities.

Authors:  A Falek; R Schmidt; G A Jervis
Journal:  Pediatrics       Date:  1966-01       Impact factor: 7.124

4.  Further delineation of the dup(3q) syndrome.

Authors:  G N Wilson; M Dasouki; M Barr
Journal:  Am J Med Genet       Date:  1985-09

5.  Chromosome 3q duplication and the Brachmann-De Lange syndrome (BDLS).

Authors:  U Francke; J M Opitz
Journal:  J Pediatr       Date:  1979-07       Impact factor: 4.406

6.  The phenotype of ring chromosome 3.

Authors:  G N Wilson; J Pooley; J Parker
Journal:  J Med Genet       Date:  1982-12       Impact factor: 6.318

7.  The association of chromosome 3 duplication and the Cornelia de Lange syndrome.

Authors:  G N Wilson; V C Hieber; R D Schmickel
Journal:  J Pediatr       Date:  1978-11       Impact factor: 4.406
  7 in total

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