Literature DB >> 17431893

The first 4p euchromatic variant in a healthy carrier having an unusual reproductive history.

L Rodríguez1, M Zollino, E Mansilla, M L Martínez-Fernández, P Pérez, M Murdolo, M L Martínez-Frías.   

Abstract

We report on the molecular cytogenetics studies in a healthy couple who had had three pregnancies which ended in a termination of pregnancy (TOP). In two of them, prenatal sonogram showed fetal dwarfism and in the third one, a chromosome alteration was found in the amniocentesis. A previous pregnancy ended in a healthy girl. A high-resolution G-band karyotype (550-850 bands), together with Fluorescence in situ Hybridization (FISH) techniques, detected in the father a 4p interstitial euchromatic duplication. This chromosome duplication appears to be a previously undescribed euchromatic variant (EV). We discuss the possibility that the 4p paternal EV could be involved in the clinical and genetic findings of the three TOPs.

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Year:  2007        PMID: 17431893     DOI: 10.1002/ajmg.a.31681

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  2 in total

1.  Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16.

Authors:  Irina Balikova; Kevin Martens; Cindy Melotte; Mustapha Amyere; Steven Van Vooren; Yves Moreau; David Vetrie; Heike Fiegler; Nigel P Carter; Thomas Liehr; Miikka Vikkula; Gert Matthijs; Jean-Pierre Fryns; Ingele Casteels; Koen Devriendt; Joris Robert Vermeesch
Journal:  Am J Hum Genet       Date:  2008-01       Impact factor: 11.025

2.  Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation.

Authors:  Bernd Auber; Verena Bruemmer; Barbara Zoll; Peter Burfeind; Detlef Boehm; Thomas Liehr; Knut Brockmann; Ekkehard Wilichowski; Loukas Argyriou; Iris Bartels
Journal:  Mol Cytogenet       Date:  2009-03-12       Impact factor: 2.009

  2 in total

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