Literature DB >> 2248305

Parental origin of del(15)(q11-q13) in Angelman and Prader-Willi syndromes.

R Zori, C Williams, J F Mattei, A Moncla.   

Abstract

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Year:  1990        PMID： 2248305     DOI： 10.1002/ajmg.1320370233

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


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  3 in total

1.  Prader-Willi or Angelman syndrome in familial 15q11----q13 deletion of maternal origin?

Authors:  A Schinzel; W P Robinson; A Bottani; X Yagang; A Prader
Journal:  Hum Genet       Date:  1992-01       Impact factor: 4.132

Review 2.  Angelman syndrome - insights into a rare neurogenetic disorder.

Authors:  Karin Buiting; Charles Williams; Bernhard Horsthemke
Journal:  Nat Rev Neurol       Date:  2016-09-12       Impact factor: 42.937

Review 3.  Clinical characteristics and epilepsy in genomic imprinting disorders: Angelman syndrome and Prader-Willi syndrome.

Authors:  Tzong-Shi Wang; Wen-Hsin Tsai; Li-Ping Tsai; Shi-Bing Wong
Journal:  Ci Ji Yi Xue Za Zhi       Date:  2019-10-31
  3 in total

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