Literature DB >> 8725798

Detection of imprinting mutations in Angelman syndrome using a probe for exon alpha of SNRPN.

J Beuten, J S Sutcliffe, B M Casey, A L Beaudet, R C Hennekam, P J Willems.   

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Year:  1996        PMID： 8725798     DOI： 10.1002/ajmg.1320630206

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  3 in total

1.  Angelman syndrome in an inbred family.

Authors:  J Beuten; R C Hennekam; B Van Roy; K Mangelschots; J S Sutcliffe; D J Halley; F A Hennekam; A L Beaudet; P J Willems
Journal:  Hum Genet       Date:  1996-03       Impact factor: 4.132

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

Review 3.  Epigenomic strategies at the interface of genetic and environmental risk factors for autism.

Authors:  Janine M LaSalle
Journal:  J Hum Genet       Date:  2013-05-16       Impact factor: 3.172
  3 in total

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