Literature DB >> 22342433

Unexpected results in the constitution of small supernumerary marker chromosomes.

Annalisa Vetro1, Emmanouil Manolakos, Michael B Petersen, Loretta Thomaidis, Thomas Liehr, Gianfranco Croci, Fabrizia Franchi, Maria Marinelli, Emanuela Meneghelli, Babara Dal Bello, Stefania Cesari, Angela Iasci, Giulia Arrigo, Orsetta Zuffardi.   

Abstract

Traditional approaches for the classification of Small Supernumerary Marker Chromosomes (sSMC), mostly based on FISH techniques, are time-consuming and not always sufficient to fully understand the true complexity of this class of rearrangements. We describe four supernumerary marker chromosomes that, after array-CGH, were interpreted rather differently in respect to the early classification made by conventional cytogenetics and FISH investigations, reporting two types of complex markers which DNA content was overlooked by conventional approaches: 1. the sSMC contains non-contiguous regions of the same chromosome and, 2. the sSMC, initially interpreted as a supernumerary del(15), turns out to be a derivative 15 to which the portion of another chromosome was attached. All are likely derived from partial trisomy rescue events, bringing further demonstration that germline chromosomal imbalances are submitted to intense reshuffling during the embryogenesis, leading to unexpected complexity and changing the present ideas on the composition of supernumerary marker chromosomes.
Copyright © 2012 Elsevier Masson SAS. All rights reserved.

Mesh:

Year:  2012        PMID: 22342433     DOI: 10.1016/j.ejmg.2012.01.010

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  13 in total

1.  APC rearrangements in familial adenomatous polyposis: heterogeneity of deletion lengths and breakpoint sequences underlies similar phenotypes.

Authors:  Marialuisa Quadri; Annalisa Vetro; Viviana Gismondi; Monica Marabelli; Lucio Bertario; Paola Sala; Liliana Varesco; Orsetta Zuffardi; Guglielmina N Ranzani
Journal:  Fam Cancer       Date:  2015-03       Impact factor: 2.375

2.  MCM5: a new actor in the link between DNA replication and Meier-Gorlin syndrome.

Authors:  Annalisa Vetro; Salvatore Savasta; Annalisa Russo Raucci; Cristina Cerqua; Geppo Sartori; Ivan Limongelli; Antonella Forlino; Silvia Maruelli; Paola Perucca; Debora Vergani; Giuliano Mazzini; Andrea Mattevi; Lucia Anna Stivala; Leonardo Salviati; Orsetta Zuffardi
Journal:  Eur J Hum Genet       Date:  2017-02-15       Impact factor: 4.246

3.  Deletions of the PRKAR1A locus at 17q24.2-q24.3 in Carney complex: genotype-phenotype correlations and implications for genetic testing.

Authors:  Paraskevi Salpea; Anelia Horvath; Edra London; Fabio R Faucz; Annalisa Vetro; Isaac Levy; Evgenia Gourgari; Andrew Dauber; Ingrid A Holm; Patrick J Morrison; Margaret F Keil; Charalampos Lyssikatos; Eric D Smith; Marc A Sanidad; JoAnn C Kelly; Zunyan Dai; Philip Mowrey; Antonella Forlino; Orsetta Zuffardi; Constantine A Stratakis
Journal:  J Clin Endocrinol Metab       Date:  2013-12-20       Impact factor: 5.958

4.  De novo unbalanced translocations have a complex history/aetiology.

Authors:  Maria Clara Bonaglia; Nehir Edibe Kurtas; Edoardo Errichiello; Sara Bertuzzo; Silvana Beri; Mana M Mehrjouy; Aldesia Provenzano; Debora Vergani; Vanna Pecile; Francesca Novara; Paolo Reho; Marilena Carmela Di Giacomo; Giancarlo Discepoli; Roberto Giorda; Micheala A Aldred; Cíntia Barros Santos-Rebouças; Andressa Pereira Goncalves; Diane N Abuelo; Sabrina Giglio; Ivana Ricca; Fabrizia Franchi; Philippos Patsalis; Carolina Sismani; María Angeles Morí; Julián Nevado; Niels Tommerup; Orsetta Zuffardi
Journal:  Hum Genet       Date:  2018-10-01       Impact factor: 4.132

5.  Gain of FAM123B and ARHGEF9 in an Obese Man with Intellectual Disability, Congenital Heart Defects and Multiple Supernumerary Ring Chromosomes.

Authors:  R Hochstenbach; M E van Gijn; P-J Krijtenburg; R Raemakers; R van 't Slot; I Renkens; M J Eleveld; J J van der Smagt; M Poot
Journal:  Mol Syndromol       Date:  2012-11-20

6.  Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors.

Authors:  Ron Hochstenbach; Beata Nowakowska; Marianne Volleth; Amber Ummels; Anna Kutkowska-Kaźmierczak; Ewa Obersztyn; Kamila Ziemkiewicz; Claudia Gerloff; Denny Schanze; Martin Zenker; Petra Muschke; Ina Schanze; Martin Poot; Thomas Liehr
Journal:  Mol Syndromol       Date:  2015-10-31

7.  Design and validation of a pericentromeric BAC clone set aimed at improving diagnosis and phenotype prediction of supernumerary marker chromosomes.

Authors:  Chiara Castronovo; Emanuele Valtorta; Milena Crippa; Sara Tedoldi; Lorenza Romitti; Maria Cristina Amione; Silvana Guerneri; Daniela Rusconi; Lucia Ballarati; Donatella Milani; Enrico Grosso; Pietro Cavalli; Daniela Giardino; Maria Teresa Bonati; Lidia Larizza; Palma Finelli
Journal:  Mol Cytogenet       Date:  2013-10-30       Impact factor: 2.009

8.  Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization.

Authors:  Mingran Sun; Han Zhang; Guiying Li; Carrie J Guy; Xianfu Wang; Xianglan Lu; Fangchao Gong; Jiyun Lee; Susan Hassed; Shibo Li
Journal:  Sci Rep       Date:  2017-09-04       Impact factor: 4.379

9.  Severe growth hormone deficiency and pituitary malformation in a patient with chromosome 2p25 duplication and 2q37 deletion.

Authors:  Annalisa Vetro; Sara Pagani; Margherita Silengo; Mariasavina Severino; Elena Bozzola; Cristina Meazza; Orsetta Zuffardi; Mauro Bozzola
Journal:  Mol Cytogenet       Date:  2014-06-19       Impact factor: 2.009

10.  Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism.

Authors:  Juliana Dourado Grzesiuk; Ciro Silveira Pereira; Carlos Henrique Paiva Grangeiro; Clarissa Gondim Picanço-Albuquerque; Flávia Gaona Oliveira-Gennaro; Filipe Brum Machado; Enrique Medina-Acosta; Ester Silveira Ramos; Maisa Yoshimoto; Lucia Martelli
Journal:  Mol Cytogenet       Date:  2016-06-15       Impact factor: 2.009

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