Literature DB >> 6167167

Resolution of breakpoints in a complex rearrangement by use of multiple staining techniques: confirmation of suspected 12p12.3 intraband by deletion dosage effect of LDHB.

E Magenis, M G Brown, J Chamberlin, T Donlon, D Hepburn, N Lamvik, E Lovrien, M Yoshitomi.   

Abstract

A complex de novo translocation was found in leukocytes and fibroblasts from a boy with mental retardation and minor abnormalities. The 45,XY chromosome constitution found in all cells was initially interpreted from routine G- and Q-banding techniques as a balanced translocation of part of the short arm of 12 to the short arm of 15 and of the long arm of 21 to the short arm of 12. With additional staining techniques and use of prometaphase chromosome preparations, it was determined that the distal portion of band 12.3 of the short arm of chromosome 12 was missing from the 12/15 and the 12/21 translocation chromosomes. This interpretation was confirmed by a decreased concentration of the LDH-B subunit in lactate dehydrogenase isozymes of the patient's fibroblasts, consistent with his being hemizygous for the LDHB locus.

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Year:  1981        PMID: 6167167     DOI: 10.1002/ajmg.1320090203

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

1.  Partial monosomy 12p13.1----13.3.

Authors:  D R Romain; J Goldsmith; L M Columbano-Green; C J Chapman; R H Smythe; R G Parfitt
Journal:  J Med Genet       Date:  1987-07       Impact factor: 6.318

2.  High resolution cytogenetic evaluation of couples with recurring fetal wastage.

Authors:  T L Yang-Feng; S C Finley; W H Finley; U Francke
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization.

Authors:  D A Batista; C M Tuck-Muller; J E Martinez; W G Kearns; P L Pearson; G Stetten
Journal:  Hum Genet       Date:  1993-09       Impact factor: 4.132

4.  Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features.

Authors:  Allen N Lamb; Jill A Rosenfeld; Nicholas J Neill; Michael E Talkowski; Ian Blumenthal; Santhosh Girirajan; Debra Keelean-Fuller; Zheng Fan; Jill Pouncey; Cathy Stevens; Loren Mackay-Loder; Deborah Terespolsky; Patricia I Bader; Kenneth Rosenbaum; Stephanie E Vallee; John B Moeschler; Roger Ladda; Susan Sell; Judith Martin; Shawnia Ryan; Marilyn C Jones; Rocio Moran; Amy Shealy; Suneeta Madan-Khetarpal; Juliann McConnell; Urvashi Surti; Andrée Delahaye; Bénédicte Heron-Longe; Eva Pipiras; Brigitte Benzacken; Sandrine Passemard; Alain Verloes; Bertrand Isidor; Cedric Le Caignec; Gwen M Glew; Kent E Opheim; Maria Descartes; Evan E Eichler; Cynthia C Morton; James F Gusella; Roger A Schultz; Blake C Ballif; Lisa G Shaffer
Journal:  Hum Mutat       Date:  2012-04       Impact factor: 4.878

Review 5.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  Methyl green is a substitute for distamycin A in the formation of distamycin A/DAPI C-bands.

Authors:  T A Donlon; R E Magenis
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

7.  Interstitial 12p deletion involving more than 40 genes in a patient with postnatal microcephaly, psychomotor delay, optic nerve atrophy, and facial dysmorphism.

Authors:  Anne Hoppe; Jan Heinemeyer; Eva Klopocki; Luitgard M Graul-Neumann; Birgit Spors; Petra Bittigau; Angela M Kaindl
Journal:  Meta Gene       Date:  2014-01-11

8.  12p deletion spectrum syndrome: a new case report reinforces the evidence regarding the potential relationship to autism spectrum disorder and related developmental impairments.

Authors:  Marcio Leyser; Bruno Leonardo Dias; Ana Luiza Coelho; Marcio Vasconcelos; Osvaldo J M Nascimento
Journal:  Mol Cytogenet       Date:  2016-10-04       Impact factor: 2.009

  8 in total

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