Literature DB >> 12503109

Muellerian aplasia associated with ring chromosome 8p12q12 mosaicism.

Judith Loeffler1, Elisabeth Soelder, Martin Erdel, Barbara Utermann, Andreas Janecke, Hans-Christoph Duba, Gerd Utermann.   

Abstract

We report on a woman with Muellerian aplasia, renal and skeletal anomalies, and minor dysmorphic signs. Conventional cytogenetic analysis revealed mosaicism for a small supernumerary, undefinable ring chromosome. Chromosome microdissection and reverse painting demonstrated that this marker contained pericentric material from chromosome 8 (8p12q12). Thus, we identified a Muellerian aplasia phenotype with partial trisomy 8 mosaicism. Copyright 2002 Wiley-Liss, Inc.

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Year:  2003        PMID: 12503109     DOI: 10.1002/ajmg.a.10902

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  2 in total

1.  Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients.

Authors:  Joanna Pietrzak; Kristin Mrasek; Ewa Obersztyn; Pawel Stankiewicz; Nadezda Kosyakova; Anja Weise; Sau Wai Cheung; Wei Wen Cai; Ferdinand von Eggeling; Tadeusz Mazurczak; Ewa Bocian; Thomas Liehr
Journal:  J Appl Genet       Date:  2007       Impact factor: 3.240

2.  First case of two supernumerary markers derived from chromosome 5 and chromosome 8.

Authors:  Roberta Giansante; Chiara Palka Bayard De Volo; Melissa Alfonsi; Elisena Morizio; Paolo Guanciali Franchi
Journal:  Mol Cytogenet       Date:  2022-06-27       Impact factor: 1.904

  2 in total

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