Literature DB >> 20063327

Maternal uniparental disomy 15 in a fetus resulting from a balanced familial translocation t(2;15)(p11;q11.2).

S Heidemann, H Plendl, I Vater, S Gesk, J R Exeler-Telker, W Grote, R Siebert, A Caliebe.   

Abstract

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Year:  2010        PMID： 20063327     DOI： 10.1002/pd.2436

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN： 0197-3851            Impact factor:   3.050


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  3 in total

1.  Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(15;19)(q12;p13.3).

Authors:  Vy Dang; Abhilasha Surampalli; Ann M Manzardo; Stephanie Youn; Merlin G Butler; June-Anne Gold; Virginia E Kimonis
Journal:  Cytogenet Genome Res       Date:  2016-11-29       Impact factor: 1.636

Review 2.  Benefits and limitations of prenatal screening for Prader-Willi syndrome.

Authors:  Merlin G Butler
Journal:  Prenat Diagn       Date:  2016-10-12       Impact factor: 3.050

3.  Prenatal diagnosis of maternal partial trisomy 9p23p24.3 and 14q11.2q21.3 in a fetus: a case report.

Authors:  J B Wu; J Sha; J F Zhai; Y Liu; B Zhang
Journal:  Mol Cytogenet       Date:  2020-02-06       Impact factor: 2.009
  3 in total

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