Literature DB >> 1923841

A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3).

P M Bouloux1, J P Hardelin, P Munroe, J M Kirk, R Legouis, J Levilliers, J Hazan, J Weissenbach, C Petit.   

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Year:  1991        PMID： 1923841      PMCID： PMC328937          DOI： 10.1093/nar/19.19.5453

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


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  1 in total

1.  Long-range restriction map of the terminal part of the short arm of the human X chromosome.

Authors:  C Petit; J Levilliers; J Weissenbach
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205
  1 in total
  5 in total

1.  Carrier detection in X linked ocular albinism using linked DNA polymorphisms.

Authors:  S J Charles; A T Moore; Y Zhang; R McMahon; D E Barton; J R Yates
Journal:  Br J Ophthalmol       Date:  1994-07       Impact factor: 4.638

2.  Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

Authors:  Y Zhang; R McMahon; S J Charles; J S Green; A T Moore; D E Barton; J R Yates
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318

3.  Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.

Authors:  S J Scheinman; M A Pook; C Wooding; J T Pang; P A Frymoyer; R V Thakker
Journal:  J Clin Invest       Date:  1993-06       Impact factor: 14.808

4.  Fulminant meningococcal septic shock in a boy with combined inherited properdin and protein C deficiency.

Authors:  C A Fijen; B H Derkx; E J Kuijper; M Mannens; S R Poort; M Peters; M R Daha; J Dankert
Journal:  Clin Exp Immunol       Date:  1995-11       Impact factor: 4.330

5.  Phenotypic variability in X-linked ocular albinism: relationship to linkage genotypes.

Authors:  R E Schnur; P A Wick; C Bailey; T Rebbeck; R G Weleber; J Wagstaff; A W Grix; R A Pagon; A Hockey; M J Edwards
Journal:  Am J Hum Genet       Date:  1994-09       Impact factor: 11.025
  5 in total

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