Literature DB >> 1685358

Identification of a marker chromosome as inv dup(15) by molecular analysis.

Y Shibuya1, H Tonoki, N Kajii, N Niikawa.   

Abstract

The origin of an extra marker chromosome in a patient with mental retardation and intractable epilepsy was ascertained by DNA analysis. Gene dose and restriction fragment length polymorphism (RFLP) studies of D15S9 proved that the patient was tetrasomic for the gene and that the extra chromosome was of maternal origin. On the basis of the molecular findings, further detailed GTG-banded chromosome analysis interpreted the marker chromosome as inv dup(15)(pter----q14::q14----pter). The clinical manifestations of the patient are consistent with those of the patients previously described.

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Year:  1991        PMID: 1685358     DOI: 10.1111/j.1399-0004.1991.tb03083.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  8 in total

1.  Maternal origin of inv dup(15) chromosomes in infantile autism.

Authors:  T Martinsson; T Johannesson; M Vujic; A Sjöstedt; S Steffenburg; C Gillberg; J Wahlström
Journal:  Eur Child Adolesc Psychiatry       Date:  1996-12       Impact factor: 4.785

Review 2.  Inv dup(15) supernumerary marker chromosomes.

Authors:  T Webb
Journal:  J Med Genet       Date:  1994-08       Impact factor: 6.318

3.  Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15.

Authors:  A E Wandstrat; J Leana-Cox; L Jenkins; S Schwartz
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

4.  Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.

Authors:  J Leana-Cox; L Jenkins; C G Palmer; R Plattner; L Sheppard; W L Flejter; J Zackowski; F Tsien; S Schwartz
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

5.  Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients.

Authors:  S D Cheng; N B Spinner; E H Zackai; J H Knoll
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

6.  A genetic model for the Prader-Willi syndrome and its implication for Angelman syndrome.

Authors:  I Kennerknecht
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

7.  Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype.

Authors:  Andras Szabo; Marta Czako; Kinga Hadzsiev; Balazs Duga; Katalin Komlosi; Bela Melegh
Journal:  Mol Cytogenet       Date:  2015-06-25       Impact factor: 2.009

8.  Complex small supernumerary marker chromosome with a 15q/16p duplication: clinical implications.

Authors:  Denise M Christofolini; Flavia B Piazzon; Carolina Evo; Fernanda A Mafra; Stella R Cosenza; Alexandre T Dias; Caio P Barbosa; Bianca Bianco; Leslie D Kulikowski
Journal:  Mol Cytogenet       Date:  2014-04-24       Impact factor: 2.009

  8 in total

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