Literature DB >> 8014973

Value of chromosome painting in determining the chromosomal outcome in offspring of a 12;16 translocation carrier.

C A Brandt1, T Lyngbye, S Pedersen, L Bolund, U Friedrich.   

Abstract

We currently use direct and reverse chromosome painting in prenatal diagnosis. In a family with a subtle 12;16 translocation, adjacent 1 segregation was diagnosed in the first child, a boy, in whom symptoms compatible with partial trisomy 16p and partial monosomy 12q were seen. In the next pregnancy, a chorionic villus biopsy was tested using chromosome painting. Only by supplementing conventional cytogenetic methods with molecular cytogenetic techniques could the true karyotype be unequivocally determined. Reverse painting, using DOP-PCR amplified, flow sorted paternal derivative chromosomes as a DNA library to paint the chorionic villus cells, was especially informative.

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Year:  1994        PMID: 8014973      PMCID: PMC1049749          DOI: 10.1136/jmg.31.3.234

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  9 in total

1.  The presence of interstitial telomeric sequences in constitutional chromosome abnormalities.

Authors:  V M Park; K M Gustashaw; T M Wathen
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

2.  Detection of subtle reciprocal translocations by fluorescence in situ hybridization.

Authors:  F Speleman; N Van Roy; J Wiegant; M R Verschraegen-Spae; Y Benoit; P Govaert; L Goossens; J G Leroy
Journal:  Clin Genet       Date:  1992-04       Impact factor: 4.438

Review 3.  Trisomy 16p in a liveborn offspring due to maternal translocation t(16;21)(q11;p11) and review of the literature.

Authors:  C Léonard; J L Huret; M C Imbert; Y Lebouc; J Selva; A M Boulley
Journal:  Am J Med Genet       Date:  1992-06-01

4.  Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics.

Authors:  A Jauch; C Daumer; P Lichter; J Murken; T Schroeder-Kurth; T Cremer
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132

5.  A highly conserved repetitive DNA sequence, (TTAGGG)n, present at the telomeres of human chromosomes.

Authors:  R K Moyzis; J M Buckingham; L S Cram; M Dani; L L Deaven; M D Jones; J Meyne; R L Ratliff; J R Wu
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

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

Review 7.  Ring chromosome 20 with loss of telomeric sequences detected by multicolour PRINS.

Authors:  C A Brandt; O Kierkegaard; J Hindkjaer; P K Jensen; S Pedersen; A J Therkelsen
Journal:  Clin Genet       Date:  1993-07       Impact factor: 4.438

8.  Pseudodicentric chromosome 18 diagnosed by chromosome painting and primed in situ labelling (PRINS).

Authors:  C A Brandt; B Djernes; H Strømkjaer; M B Petersen; S Pedersen; J Hindkjaer; J Brinch-Iversen; G Bruun-Petersen
Journal:  J Med Genet       Date:  1994-02       Impact factor: 6.318

9.  Cytogenetic analysis by chromosome painting using DOP-PCR amplified flow-sorted chromosomes.

Authors:  H Telenius; A H Pelmear; A Tunnacliffe; N P Carter; A Behmel; M A Ferguson-Smith; M Nordenskjöld; R Pfragner; B A Ponder
Journal:  Genes Chromosomes Cancer       Date:  1992-04       Impact factor: 5.006

  9 in total
  2 in total

1.  "Molecular rulers" for calibrating phenotypic effects of telomere imbalance.

Authors:  C L Martin; D J Waggoner; A Wong; S Uhrig; J A Roseberry; J F Hedrick; S D Pack; K Russell; E Zackai; W B Dobyns; D H Ledbetter
Journal:  J Med Genet       Date:  2002-10       Impact factor: 6.318

Review 2.  Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literature.

Authors:  Brian P Brooks; Jeanne M Meck; Bassem R Haddad; Claude Bendavid; Delphine Blain; Jeffrey A Toretsky
Journal:  BMC Med Genet       Date:  2006-01-13       Impact factor: 2.103

  2 in total

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