Literature DB >> 1347469

The p locus is closely linked to the mouse homolog of a gene from the Prader-Willi chromosomal region.

Y Nakatsu1, Y Gondo, M H Brilliant.   

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Year:  1992        PMID： 1347469     DOI： 10.1007/bf00570442

Source DB:  PubMed          Journal:  Mamm Genome        ISSN： 0938-8990            Impact factor:   2.957


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  24 in total

1.  Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR).

Authors:  A J Kirkilionis; C A Gregory; J L Hamerton
Journal:  Genomics       Date:  1991-03       Impact factor: 5.736

2.  Statistical considerations for linkage analysis using recombinant inbred strains and backcrosses.

Authors:  J Silver; C E Buckler
Journal:  Proc Natl Acad Sci U S A       Date:  1986-03       Impact factor: 11.205

Review 3.  Recurrence risk in the Angelman ("happy puppet") syndrome.

Authors:  P J Willems; I Dijkstra; O F Brouwer; G P Smit
Journal:  Am J Med Genet       Date:  1987-08

4.  Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome.

Authors:  T A Donlon; M Lalande; A Wyman; G Bruns; S A Latt
Journal:  Proc Natl Acad Sci U S A       Date:  1986-06       Impact factor: 11.205

5.  Direct molecular identification of the mouse pink-eyed unstable mutation by genome scanning.

Authors:  M H Brilliant; Y Gondo; E M Eicher
Journal:  Science       Date:  1991-04-26       Impact factor: 47.728

6.  Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome.

Authors:  U Tantravahi; R D Nicholls; H Stroh; S Ringer; R L Neve; L Kaplan; R Wharton; D Wurster-Hill; J M Graham; E S Cantú
Journal:  Am J Med Genet       Date:  1989-05

7.  Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences.

Authors:  R E Magenis; S Toth-Fejel; L J Allen; M Black; M G Brown; S Budden; R Cohen; J M Friedman; D Kalousek; J Zonana
Journal:  Am J Med Genet       Date:  1990-03

8.  Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.

Authors:  C A Williams; R T Zori; J W Stone; B A Gray; E S Cantu; H Ostrer
Journal:  Am J Med Genet       Date:  1990-03

9.  Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.

Authors:  M G Butler
Journal:  Am J Hum Genet       Date:  1989-07       Impact factor: 11.025

10.  Hypopigmentation in the Prader-Willi syndrome.

Authors:  G L Wiesner; C M Bendel; D P Olds; J G White; D C Arthur; D W Ball; R A King
Journal:  Am J Hum Genet       Date:  1987-05       Impact factor: 11.025
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  6 in total

1.  The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12.

Authors:  M Ramsay; M A Colman; G Stevens; E Zwane; J Kromberg; M Farrall; T Jenkins
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025

2.  Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse.

Authors:  M F Lyon; T R King; Y Gondo; J M Gardner; Y Nakatsu; E M Eicher; M H Brilliant
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-01       Impact factor: 11.205

3.  The tyrosinase-positive oculocutaneous albinism gene shows locus homogeneity on chromosome 15q11-q13 and evidence of multiple mutations in southern African negroids.

Authors:  M A Kedda; G Stevens; P Manga; C Viljoen; T Jenkins; M Ramsay
Journal:  Am J Hum Genet       Date:  1994-06       Impact factor: 11.025

Review 4.  The mouse pink-eyed dilution locus: a model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito.

Authors:  M H Brilliant
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

5.  Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse.

Authors:  R D Nicholls; W Gottlieb; L B Russell; M Davda; B Horsthemke; E M Rinchik
Journal:  Proc Natl Acad Sci U S A       Date:  1993-03-01       Impact factor: 11.205

6.  High-frequency genetic reversion mediated by a DNA duplication: the mouse pink-eyed unstable mutation.

Authors:  Y Gondo; J M Gardner; Y Nakatsu; D Durham-Pierre; S A Deveau; C Kuper; M H Brilliant
Journal:  Proc Natl Acad Sci U S A       Date:  1993-01-01       Impact factor: 11.205
  6 in total

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