Literature DB >> 2891112

RFLP of the human placental alkaline phosphatase gene (PLAP).

D Martin1, N K Spurr, J Trowsdale.   

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Year:  1987        PMID： 2891112      PMCID： PMC306450          DOI： 10.1093/nar/15.21.9104

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


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  2 in total

1.  Pst I restriction fragment length polymorphism of the human placental alkaline phosphatase gene in normal placentae and tumors.

Authors:  L Tsavaler; R C Penhallow; W Kam; H H Sussman
Journal:  Proc Natl Acad Sci U S A       Date:  1987-07       Impact factor: 11.205

2.  The human placental alkaline phosphatase gene and related sequences map to chromosome 2 band q37.

Authors:  D Martin; D F Tucker; P Gorman; D Sheer; N K Spurr; J Trowsdale
Journal:  Ann Hum Genet       Date:  1987-05       Impact factor: 1.670
  2 in total
  5 in total

1.  Pst I restriction fragment length polymorphism of human placental alkaline phosphatase gene: Mendelian segregation and localization of mutation site in the gene.

Authors:  L Tsavaler; R C Penhallow; H H Sussman
Journal:  Proc Natl Acad Sci U S A       Date:  1988-10       Impact factor: 11.205

2.  DNA polymorphism of alkaline phosphatase isozyme genes: linkage disequilibria between placental and germ-cell alkaline phosphatase alleles.

Authors:  G Beckman; L Beckman; C Sikström; J L Millán
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

3.  Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse.

Authors:  C Foy; V Newton; D Wellesley; R Harris; A P Read
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

4.  Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.

Authors:  L A Farrer; K S Arnos; J H Asher; C T Baldwin; S R Diehl; T B Friedman; J Greenberg; K M Grundfast; C Hoth; A K Lalwani
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

5.  Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.

Authors:  L A Farrer; K M Grundfast; J Amos; K S Arnos; J H Asher; P Beighton; S R Diehl; J Fex; C Foy; T B Friedman
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025
  5 in total

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