Literature DB >> 18509863

Prenatal diagnosis of a fetus with 7q11.23 deletion detected by multiplex ligation-dependent probe amplification (MLPA) screening.

Harry Kontos, Emmanouil Manolakos, Pantelis Malligiannis, Nicolaos Plachouras, Nikolaos Ploumis, Markos Mihalatos, Sandro Orru, Ema Anastasiadou, Michael B Petersen.   

Abstract

Mesh：

Year:  2008        PMID： 18509863     DOI： 10.1002/pd.2020

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


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  2 in total

1.  Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis.

Authors:  Ruibin Huang; Hang Zhou; Fang Fu; Ru Li; Tingying Lei; Yingsi Li; Ken Cheng; You Wang; Xin Yang; Lushan Li; Xiangyi Jing; Yongling Zhang; Fucheng Li; Dongzhi Li; Can Liao
Journal:  Mol Cytogenet       Date:  2022-06-28       Impact factor: 1.904

2.  Prenatal phenotype of Williams-Beuren syndrome and of the reciprocal duplication syndrome.

Authors:  Livia Marcato; Licia Turolla; Eva Pompilii; Celine Dupont; Nicolas Gruchy; Simona De Toffol; Gabriella Bracalente; Severine Bacrot; Enzo Troilo; Anne C Tabet; Sabrina Rossi; Anne L Delezoïde; Demetrio Baldo; Nathalie Leporrier; Federico Maggi; Arnaud Molin; Gianluigi Pilu; Giuseppe Simoni; Francois Vialard; Francesca R Grati
Journal:  Clin Case Rep       Date:  2014-02-06
  2 in total

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