Literature DB >> 2027784

Dinucleotide repeat polymorphism at the PGK1 locus.

D L Browne1, J Zonana, M Litt.   

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Year:  1991        PMID： 2027784      PMCID： PMC333956     

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


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  3 in total

1.  Five polymorphic microsatellite VNTRs on the human X chromosome.

Authors:  J A Luty; Z Guo; H F Willard; D H Ledbetter; S Ledbetter; M Litt
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

Review 2.  Report of the committee on the genetic constitution of the X chromosome.

Authors:  J L Mandel; H F Willard; R L Nussbaum; G Romeo; J M Puck; K E Davies
Journal:  Cytogenet Cell Genet       Date:  1989

3.  Restriction site polymorphism in the phosphoglycerate kinase gene on the X chromosome.

Authors:  M H Hutz; A M Michelson; S E Antonarakis; S H Orkin; H H Kazazian
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132
  3 in total
  4 in total

1.  Dinucleotide repeat polymorphism at the PGK1P1 locus.

Authors:  D L Browne; J Zonana; M Litt
Journal:  Nucleic Acids Res       Date:  1992-03-11       Impact factor: 16.971

2.  High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus.

Authors:  J Zonana; M Jones; D Browne; M Litt; P Kramer; H W Becker; N Brockdorff; S Rastan; K P Davies; A Clarke
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

3.  Arginine-164-tryptophan substitution in connexin32 associated with X linked dominant Charcot-Marie-Tooth disease.

Authors:  A Oterino; F I Montón; V M Cabrera; F Pinto; A Gonzalez; N R Lavilla
Journal:  J Med Genet       Date:  1996-05       Impact factor: 6.318

4.  X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphisms.

Authors:  S Cochrane; J Bergoffen; N D Fairweather; E Müller; M L Mostacciuolo; A P Monaco; K H Fischbeck; N E Haites
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318
  4 in total

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