Literature DB >> 1301155

Dinucleotide repeat polymorphism at the D15S11 locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15.

A Mutirangura1, A Kuwano, S A Ledbetter, A C Chinault, D H Ledbetter.   

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Year:  1992        PMID： 1301155     DOI： 10.1093/hmg/1.2.139-a

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


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  17 in total

1.  Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome families.

Authors:  H L Gilbert; J L Buxton; C T Chan; T McKay; S Cottrell; S Ramsden; R M Winter; M E Pembrey; S Malcolm
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

2.  Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.

Authors:  V Greger; J H Knoll; J Wagstaff; E Woolf; P Lieske; H Glatt; P A Benn; S S Rosengren; M Lalande
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

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

4.  Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb.

Authors:  S L Christian; N K Bhatt; S A Martin; J S Sutcliffe; T Kubota; B Huang; A Mutirangura; A C Chinault; A L Beaudet; D H Ledbetter
Journal:  Genome Res       Date:  1998-02       Impact factor: 9.043

5.  Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

Authors:  A Mutirangura; F Greenberg; M G Butler; S Malcolm; R D Nicholls; A Chakravarti; D H Ledbetter
Journal:  Hum Mol Genet       Date:  1993-02       Impact factor: 6.150

6.  A molecular and cytogenetic study in Finnish Prader-Willi patients.

Authors:  H Kokkonen; M Kähkönen; J Leisti
Journal:  Hum Genet       Date:  1995-05       Impact factor: 4.132

7.  Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.

Authors:  A Reis; B Dittrich; V Greger; K Buiting; M Lalande; G Gillessen-Kaesbach; M Anvret; B Horsthemke
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

8.  Familial unbalanced translocation t(8;15)(p23.3;q11) with uniparental disomy in Angelman syndrome.

Authors:  A Smith; Z M Deng; R Beran; T Woodage; R J Trent
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

9.  Deletion breakpoints associated with the Prader-Willi and Angelman syndromes (15q11-q13) are not sites of high homologous recombination.

Authors:  W P Robinson; R Spiegel; A A Schinzel
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

10.  Linkage analysis in familial Angelman syndrome.

Authors:  J Wagstaff; Y Y Shugart; M Lalande
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025
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