(Q56377059)

English

Telomere-telomere (end to end) fusion of chromosomes 7 and 22 with an interstitial deletion of chromosome 7p11.2-->p15.1: phenotypic consequences and possible mechanisms

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scholarly article

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Telomere-telomere (end to end) fusion of chromosomes 7 and 22 with an interstitial deletion of chromosome 7p11.2-->p15.1: phenotypic consequences and possible mechanisms (English)

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author name string

S M Zneimer

1

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P D Cotter

2

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S D Stewart

3

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language of work or name

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publication date

August 2000

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Clinical Genetics

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58

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2

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129-33

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The Behavior in Successive Nuclear Divisions of a Chromosome Broken at Meiosis

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A genetic analysis of dicentric minichromosomes in Saccharomyces cerevisiae

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Chromosome stability is maintained by short intercentromeric distance in functionally dicentric human Robertsonian translocations

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Stable dicentric X chromosomes with two functional centromeres.

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Dicentric chromosomes and the inactivation of the centromere

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Telomeric associations in the progression of chromosome aberrations in pediatric solid tumors.

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Six cases of 7p deletion: Clinical, cytogenetic, and molecular studies

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Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality.

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Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13.

1 reference

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Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7p

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Identifiers

10.1034/J.1399-0004.2000.580207.X

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