Literature DB >> 10733242

A further Angelman syndrome patient with UPD15 due to paternal meiosis II nondisjunction.

C Fridman, M Santos, I Ferrari, C P Koiffmann.   

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Year:  2000        PMID： 10733242     DOI： 10.1034/j.1399-0004.2000.570114.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  1 in total

1.  Distinct phenotypes distinguish the molecular classes of Angelman syndrome.

Authors:  A C Lossie; M M Whitney; D Amidon; H J Dong; P Chen; D Theriaque; A Hutson; R D Nicholls; R T Zori; C A Williams; D J Driscoll
Journal:  J Med Genet       Date:  2001-12       Impact factor: 6.318
  1 in total

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