Trisomy of medial 15q as result of an analphoid supernumerary ring chromosome detected by CGH and FISH

No abstract is available for this paper.

• Publication year

  2007

• Venue

  Cytogenetic and Genome Research

• Publication date

  2007-12-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1159/000109635PMID 18160798
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  2005cited by this paper
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  2004cited by this paper
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  2004cited by this paper
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  2003cited by this paper
• Molecular cytogenetic techniques in detecting subtle chromosomal imbalances.

  2003cited by this paper
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  2002cited by this paper
• Genome architecture, rearrangements and genomic disorders.

  2002cited by this paper
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  2001cited by this paper
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  2000cited by this paper
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  2000cited by this paper
• Human centromeres and neocentromeres show identical distribution patterns of >20 functionally important kinetochore-associated proteins.

  2000influential reference
• Duplication of medial 15q confirmed by FISH

  2000influential reference
• FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature.

  1998influential reference
• Identification of an unusual marker chromosome by spectral karyotyping.

  1998cited by this paper
• Mosaic tetrasomy 15q25-->qter in a newborn infant with multiple anomalies.

  1996cited by this paper
• Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA.

  1994influential reference
• Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization

  1993influential reference
• A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein: activation of a latent centromere?

  1993cited by this paper
• Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes.

  1992influential reference
• Familial t(8;15)(p23.3;q22.3): report of two cases with dup(15) (q22.3----qter).

  1987cited by this paper
• Distal 15q trisomy: phenotypic comparison of nine cases in an extended family.

  1984influential reference
• A complex chromosome rearrangement resulting in trisomy 15q22→qter

  1982cited by this paper
• A complex chromosome rearrangement resulting in trisomy 15q22 to qter.

  1982cited by this paper
• A de novo tandem duplication 15(q21→qter) mosaic

  1982cited by this paper
• A de novo tandem duplication 15(q21 leads to qter) mosaic.

  1982cited by this paper

• Clinical pre‐ and postnatal (step‐by‐step) history of a boy with unbalanced translocation—t(3;15)(q26.33;q26.1)

  2011cites this paper