Literature DB >> 16931594

Application of multicolor banding for identification of complex chromosome 18 rearrangements.

Jie Hu1, Malini Sathanoori, Sally J Kochmar, Urvashi Surti.   

Abstract

Multicolor chromosome banding (mBAND) is a recently developed technique that allows the delineation of chromosomal regions with a resolution of a few megabase pairs. The resolution of mBAND is slightly below that of conventional chromosome banding; however, the color bands have a great value in identifying chromosomal abnormalities, particularly complex chromosome rearrangements, and intrachromosome exchanges (ie, inversions, deletions, duplications, and insertions). These abnormalities cannot be defined easily by conventional cytogenetic analysis or chromosome paint. In this report, we present the application of the mBAND analysis for identification of complex intrachromosome rearrangements of chromosome 18 in a child with dysmorphic features.

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Year:  2006        PMID: 16931594      PMCID: PMC1867622          DOI: 10.2353/jmoldx.2006.060001

Source DB:  PubMed          Journal:  J Mol Diagn        ISSN: 1525-1578            Impact factor:   5.568


  7 in total

1.  Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q.

Authors:  J D Cody; P D Ghidoni; B R DuPont; D E Hale; S G Hilsenbeck; R F Stratton; D S Hoffman; S Muller; R L Schaub; R J Leach; C I Kaye
Journal:  Am J Med Genet       Date:  1999-08-27

2.  High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomes.

Authors:  I Chudoba; A Plesch; T Lörch; J Lemke; U Claussen; G Senger
Journal:  Cytogenet Cell Genet       Date:  1999

3.  Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18.

Authors:  P Stankiewicz; I Brozek; Z Hélias-Rodzewicz; J Wierzba; J Pilch; E Bocian; A Balcerska; A Wozniak; I Kardaś; J Wirth; T Mazurczak; J Limon
Journal:  Am J Med Genet       Date:  2001-07-01

4.  A new chromosome banding technique, spectral color banding (SCAN), for full characterization of chromosomal abnormalities.

Authors:  Naoki Kakazu; Irit Bar-Am; Satoshi Hada; Hiroatsu Ago; Tatsuo Abe
Journal:  Genes Chromosomes Cancer       Date:  2003-08       Impact factor: 5.006

5.  Multicolor spectral karyotyping of human chromosomes.

Authors:  E Schröck; S du Manoir; T Veldman; B Schoell; J Wienberg; M A Ferguson-Smith; Y Ning; D H Ledbetter; I Bar-Am; D Soenksen; Y Garini; T Ried
Journal:  Science       Date:  1996-07-26       Impact factor: 47.728

6.  Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

Authors:  D Pinkel; J Landegent; C Collins; J Fuscoe; R Segraves; J Lucas; J Gray
Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

7.  Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH.

Authors:  Joris A Veltman; Yvonne Jonkers; Inge Nuijten; Irene Janssen; Walter van der Vliet; Erik Huys; Joris Vermeesch; Griet Van Buggenhout; Jean-Pierre Fryns; Ronald Admiraal; Paulien Terhal; Didier Lacombe; Ad Geurts van Kessel; Dominique Smeets; Eric F P M Schoenmakers; Conny M van Ravenswaaij-Arts
Journal:  Am J Hum Genet       Date:  2003-05-09       Impact factor: 11.025

  7 in total
  4 in total

1.  Multicolor banding remains an important adjunct to array CGH and conventional karyotyping.

Authors:  Susan M Bint; Angela F Davies; Caroline Mackie Ogilvie
Journal:  Mol Cytogenet       Date:  2013-12-05       Impact factor: 2.009

2.  Genome-wide association study identified CNP12587 region underlying height variation in Chinese females.

Authors:  Yin-Ping Zhang; Fei-Yan Deng; Tie-Lin Yang; Feng Zhang; Xiang-Ding Chen; Hui Shen; Xue-Zheng Zhu; Qing Tian; Hong-Wen Deng
Journal:  PLoS One       Date:  2012-09-05       Impact factor: 3.240

3.  Three supernumerary marker chromosomes in a patient with developmental delay, mental retardation, and dysmorphic features.

Authors:  Jie Hu; Suneeta Madan-Khetarpal; Alvaro H Serrano Russi; Sally Kochmar; Stephanie J Deward; Malini Sathanoori; Urvashi Surti
Journal:  Genet Res Int       Date:  2011-07-17

4.  Recombinant Chromosomes Resulting From Parental Pericentric Inversions-Two New Cases and a Review of the Literature.

Authors:  Thomas Liehr; Anja Weise; Kristin Mrasek; Monika Ziegler; Niklas Padutsch; Kathleen Wilhelm; Ahmed Al-Rikabi
Journal:  Front Genet       Date:  2019-11-14       Impact factor: 4.599

  4 in total

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