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Comment
. 2010 Feb;18(2):154-5; author reply 155-6.
doi: 10.1038/ejhg.2009.170. Epub 2009 Oct 7.

Prader-Willi and Angelman syndromes: genetic counseling

Cristina Camprubí, Maria Dolors Coll, Elisabeth Gabau, Míriam Guitart
Comment

Prader-Willi and Angelman syndromes: genetic counseling

Cristina Camprubí et al. Eur J Hum Genet. 2010 Feb.
No abstract available

PubMed Disclaimer

Comment on

  • Prader-Willi syndrome.
    Cassidy SB, Driscoll DJ. Cassidy SB, et al. Eur J Hum Genet. 2009 Jan;17(1):3-13. doi: 10.1038/ejhg.2008.165. Epub 2008 Sep 10. Eur J Hum Genet. 2009. PMID: 18781185 Free PMC article.
  • Angelman syndrome (AS, MIM 105830).
    Van Buggenhout G, Fryns JP. Van Buggenhout G, et al. Eur J Hum Genet. 2009 Nov;17(11):1367-73. doi: 10.1038/ejhg.2009.67. Epub 2009 May 20. Eur J Hum Genet. 2009. PMID: 19455185 Free PMC article. Review.

References

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    1. Van Buggenhout G, Fryns JP.Angelman syndrome (AS, MIM 105830) Eur J Hum Genet 2009. May 20 [Epub ahead of print]. - PMC - PubMed
    1. Rego A, Coll MD, Regal M, Guitart M, Escudero T, García-Mayor RV. A case with 47,XXY,del(15)(q11;q13) karyotype associated with Prader-Willi phenotype. Horm Res. 1997;48:44–46. - PubMed
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    1. Liehr T, Weise A. Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics. Int J Mol Med. 2007;19:719–731. - PubMed