Literature DB >> 1973841

Dinucleotide repeat polymorphisms at the D7S435 and D7S440 loci.

J L Weber1, A E Kwitek, P E May.   

Abstract

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Year:  1990        PMID： 1973841      PMCID： PMC331152          DOI： 10.1093/nar/18.13.4039

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  1 in total

1.  Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction.

Authors:  J L Weber; P E May
Journal:  Am J Hum Genet       Date:  1989-03       Impact factor: 11.025
  1 in total
  4 in total

1.  Substitution of aspartate for glycine 1018 in the type III procollagen (COL3A1) gene causes type IV Ehlers-Danlos syndrome: the mutated allele is present in most blood leukocytes of the asymptomatic and mosaic mother.

Authors:  S Kontusaari; G Tromp; H Kuivaniemi; C Stolle; F M Pope; D J Prockop
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

2.  Chromosome 7 suppresses indefinite division of nontumorigenic immortalized human fibroblast cell lines KMST-6 and SUSM-1.

Authors:  T Ogata; D Ayusawa; M Namba; E Takahashi; M Oshimura; M Oishi
Journal:  Mol Cell Biol       Date:  1993-10       Impact factor: 4.272

3.  Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9).

Authors:  C F Inglehearn; T J Keen; M al-Maghtheh; C Y Gregory; M R Jay; A T Moore; A C Bird; S S Bhattacharya
Journal:  Am J Hum Genet       Date:  1994-04       Impact factor: 11.025

4.  Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.

Authors:  F A Eggerding; S A Schonberg; F F Chehab; M E Norton; V A Cox; C J Epstein
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025
  4 in total

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