Literature DB >> 2676384

Report of the committee on clinical disorders and chromosomal deletion syndromes.

P S Harper, J Frézal, M A Ferguson-Smith, A Schinzel.   

Abstract

Mesh：

Year:  1989        PMID： 2676384     DOI： 10.1159/000132808

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


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  7 in total

1.  Twenty-seven nonoverlapping zinc finger cDNAs from human T cells map to nine different chromosomes with apparent clustering.

Authors:  K Huebner; T Druck; C M Croce; H J Thiesen
Journal:  Am J Hum Genet       Date:  1991-04       Impact factor: 11.025

Review 2.  Mouse chromosome 7.

Authors:  E M Rinchik; A M Saunders; B Holdener-Kenny; M J Sutcliffe; K A Brown; S D Brown; J Peters
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

3.  Localisation of the MRX3 gene for non-specific X linked mental retardation.

Authors:  A Gedeon; B Kerr; J Mulley; G Turner
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

4.  High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers.

Authors:  D F Barker; P R Fain; D E Goldgar; J N Dietz-Band; A E Turco; C E Kashtan; M C Gregory; K Tryggvason; M H Skolnick; C L Atkin
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

5.  Cloning and characterization of a 3-methyladenine DNA glycosylase cDNA from human cells whose gene maps to chromosome 16.

Authors:  L Samson; B Derfler; M Boosalis; K Call
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-15       Impact factor: 11.205

Review 6.  Diagnostic approaches to renal genetic disorders using DNA analysis.

Authors:  C A Francomano
Journal:  Pediatr Nephrol       Date:  1992-01       Impact factor: 3.714

7.  Predictive diagnosis of myotonic dystrophy with flanking microsatellite markers.

Authors:  J C Mulley; A K Gedeon; S J White; E A Haan; R I Richards
Journal:  J Med Genet       Date:  1991-07       Impact factor: 6.318
  7 in total

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