Literature DB >> 11241494

Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy.

B M Anderlid1, S Sahlén, J Schoumans, E Holmberg, I Ahsgren, G Mortier, F Speleman, E Blennow.   

Abstract

Twelve patients with varying degrees of mosaicism for a supernumerary ring chromosome were studied. The ring chromosomes were characterized using microdissection in combination with degenerate nucleotide-primed polymerase chain reaction (PCR) and reverse painting (micro-FISH). This method made it possible to determine the chromosomal origin of the ring chromosomes in detail, and thus to compare the phenotypes of similar cases. Eleven of the marker chromosomes were derived from the most proximal part of 1p, 3p, 3q, 5p, 7q, 8p, 8q, 9p, 10p and 20p. One marker chromosome had a complex origin, including the proximal and the most distal part of 20q. Eight of the families were also investigated for uniparental disomy (UPD) using microsatellite analysis. One case with maternal UPD 9 was found in a child with a ring chromosome derived from chromosome 9, r(9)(p10p12). Copyright 2001 Wiley-Liss. Inc.

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Year:  2001        PMID: 11241494     DOI: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1146>3.0.co;2-w

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


  12 in total

1.  Molecular-cytogenetic characterization of the origin and the presence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs).

Authors:  T Liehr; G Hickmann; P Kozlowski; U Claussen; H Starke
Journal:  Chromosome Res       Date:  2004       Impact factor: 5.239

Review 2.  Reverse painting highlights the origin of chromosome aberrations.

Authors:  Elisabeth Blennow
Journal:  Chromosome Res       Date:  2004       Impact factor: 5.239

3.  Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.

Authors:  M D Graf; L Christ; J T Mascarello; P Mowrey; M Pettenati; G Stetten; P Storto; U Surti; D L Van Dyke; G H Vance; D Wolff; S Schwartz
Journal:  J Med Genet       Date:  2006-08       Impact factor: 6.318

4.  Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues.

Authors:  Erin L Baldwin; Lorraine F May; April N Justice; Christa L Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2008-02       Impact factor: 11.025

Review 5.  Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances.

Authors:  Joana Barbosa Melo; Liesbeth Backx; Joris R Vermeesch; Heloisa G Santos; Ana C Sousa; Nadezda Kosyakova; Anja Weise; Ferdinand von Eggeling; Thomas Liehr; Isabel Marques Carreira
Journal:  J Appl Genet       Date:  2011-03-25       Impact factor: 3.240

Review 6.  Chromosome abnormalities without phenotypic consequences.

Authors:  Małgorzata Kowalczyk; Małgorzata Srebniak; Agnieszka Tomaszewska
Journal:  J Appl Genet       Date:  2007       Impact factor: 3.240

7.  Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients.

Authors:  Joanna Pietrzak; Kristin Mrasek; Ewa Obersztyn; Pawel Stankiewicz; Nadezda Kosyakova; Anja Weise; Sau Wai Cheung; Wei Wen Cai; Ferdinand von Eggeling; Tadeusz Mazurczak; Ewa Bocian; Thomas Liehr
Journal:  J Appl Genet       Date:  2007       Impact factor: 3.240

8.  Genomic characterization of chromosome 8 pericentric trisomy.

Authors:  Juliana H Vander Pluym; Julia O'Sullivan; Gail Andrew; Francois V Bolduc
Journal:  Clin Case Rep       Date:  2015-05-20

9.  Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier.

Authors:  Anna Mantzouratou; Anastasia Mania; Marianna Apergi; Sarah Laver; Paul Serhal; Jda Delhanty
Journal:  Mol Cytogenet       Date:  2009-01-23       Impact factor: 2.009

10.  Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?

Authors:  Vladimir Trifonov; Simon Fluri; Franz Binkert; Adayapalam Nandini; Jasen Anderson; Laura Rodriguez; Madeleine Gross; Nadezda Kosyakova; Hasmik Mkrtchyan; Elisabeth Ewers; Daniela Reich; Anja Weise; Thomas Liehr
Journal:  Mol Cytogenet       Date:  2008-04-15       Impact factor: 2.009

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