ArticleJournal of medical genetics1998
A new approach to the elucidation of complex chromosome rearrangements illustrated by a case of Rieger syndrome.
Article in Journal of medical genetics, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
3 citing papers in PubMed.
- Meiotic outcomes of three-way translocations ascertained in cleavage-stage embryos: refinement of reproductive risks and implications for PGD.European journal of human genetics : EJHG · 2014Article
- Micro-array analyses decipher exceptional complex familial chromosomal rearrangement.Human genetics · 2006Article
- A new case of an interstitial deletion (4)(q25q27) characterised by molecular cytogenetic techniques and review of the literature.European journal of pediatrics · 2003Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
A patient with a complex chromosome rearrangement and unilateral Rieger syndrome is presented. This rearrangement involves four chromosomes and six breakpoints, one of which is at 4q25, the candidate region for Rieger syndrome. We discuss a novel approach to the elucidation of this case using a multiprobe fluorescence in situ hybridisation method to show rearrangements unpredictable from G banded analysis, and the clear and unambiguous presentation of the karyotype using computer generated colour ideograms.
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Registered trials
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