Literature DB >> 18436995

Recombinant chromosome 14 due to maternal pericentric inversion.

Vytautas Sliuzas1, Algirdas Utkus, Vaidutis Kucinskas.   

Abstract

Chromosome 14 is often involved in various chromosome rearrangements, most of them balanced. Human chromosome 14 is acrocentric, so its pericentric inversions are extremely rare (only few cases have been described in the literature). Here we report on a boy with congenital malformations and recombinant chromosome 14 inherited from his mother carrying a pericentric inversion. The proband's G-banded chromosome analysis revealed derivative chromosome 14. Comparative genomic hybridization analysis identified duplication of the terminal part of chromosome 14q ish cgh dup(14)(q32.1qter). This abnormality has been confirmed by custom BAC FISH analysis. His mother's karyotype was 46,XX,inv(14)(p11.2q32.1).

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Year:  2008        PMID: 18436995     DOI: 10.1007/BF03195614

Source DB:  PubMed          Journal:  J Appl Genet        ISSN: 1234-1983            Impact factor:   3.240


  5 in total

1.  Distal 14q trisomy due to a maternal derivative chromosome 14.

Authors:  T Sonoda; K Kouno; K Sawada; T Sugimoto
Journal:  Pediatr Int       Date:  2001-06       Impact factor: 1.524

2.  The DNA sequence and analysis of human chromosome 14.

Authors:  Roland Heilig; Ralph Eckenberg; Jean-Louis Petit; Núria Fonknechten; Corinne Da Silva; Laurence Cattolico; Michaël Levy; Valérie Barbe; Véronique de Berardinis; Abel Ureta-Vidal; Eric Pelletier; Virginie Vico; Véronique Anthouard; Lee Rowen; Anup Madan; Shizhen Qin; Hui Sun; Hui Du; Kymberlie Pepin; François Artiguenave; Catherine Robert; Corinne Cruaud; Thomas Brüls; Olivier Jaillon; Lucie Friedlander; Gaelle Samson; Philippe Brottier; Susan Cure; Béatrice Ségurens; Franck Anière; Sylvie Samain; Hervé Crespeau; Nissa Abbasi; Nathalie Aiach; Didier Boscus; Rachel Dickhoff; Monica Dors; Ivan Dubois; Cynthia Friedman; Michel Gouyvenoux; Rose James; Anuradha Madan; Barbara Mairey-Estrada; Sophie Mangenot; Nathalie Martins; Manuela Ménard; Sophie Oztas; Amber Ratcliffe; Tristan Shaffer; Barbara Trask; Benoit Vacherie; Chadia Bellemere; Caroline Belser; Marielle Besnard-Gonnet; Delphine Bartol-Mavel; Magali Boutard; Stéphanie Briez-Silla; Stephane Combette; Virginie Dufossé-Laurent; Carolyne Ferron; Christophe Lechaplais; Claudine Louesse; Delphine Muselet; Ghislaine Magdelenat; Emilie Pateau; Emmanuelle Petit; Peggy Sirvain-Trukniewicz; Arnaud Trybou; Nathalie Vega-Czarny; Elodie Bataille; Elodie Bluet; Isabelle Bordelais; Maria Dubois; Corinne Dumont; Thomas Guérin; Sébastien Haffray; Rachid Hammadi; Jacqueline Muanga; Virginie Pellouin; Dominique Robert; Edith Wunderle; Gilbert Gauguet; Alice Roy; Laurent Sainte-Marthe; Jean Verdier; Claude Verdier-Discala; LaDeana Hillier; Lucinda Fulton; John McPherson; Fumihiko Matsuda; Richard Wilson; Claude Scarpelli; Gábor Gyapay; Patrick Wincker; William Saurin; Francis Quétier; Robert Waterston; Leroy Hood; Jean Weissenbach
Journal:  Nature       Date:  2003-01-01       Impact factor: 49.962

3.  A paternally derived inverted duplication of distal 14q with a terminal 14q deletion.

Authors:  Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Tzu-Hao Wang; Chen-Chi Lee; Chen-Wen Pan; Lie-Jiau Hsieh; Wayseen Wang
Journal:  Am J Med Genet A       Date:  2005-12-01       Impact factor: 2.802

4.  A novel pericentric inversion of chromosome 14 involving the rRNA gene cluster.

Authors:  Natalia T Leach; Suzanne M Cole; Deborah J Sandstrom; Stanislawa Weremowicz
Journal:  Prenat Diagn       Date:  2005-07       Impact factor: 3.050

5.  Automatic correction of the interfering effect of unsuppressed interspersed repetitive sequences in comparative genomic hybridization analysis.

Authors:  M Kirchhoff; T Gerdes; J Maahr; H Rose; C Lundsteen
Journal:  Cytometry       Date:  1997-06-01
  5 in total
  2 in total

1.  Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion.

Authors:  Hande Küçük Kurtulgan; Leyla Özer; Malik Ejder Yıldırım; Evrim Ünsal; Süleyman Aktuna; Volkan Baltacı; Nejmiye Akkuş; İlhan Sezgin
Journal:  Mol Cytogenet       Date:  2015-11-21       Impact factor: 2.009

Review 2.  A Recurrent De Novo Terminal Duplication of 14q32 in Korean Siblings Associated with Developmental Delay and Intellectual Disability, Growth Retardation, Facial Dysmorphism, and Cerebral Infarction: A Case Report and Literature Review.

Authors:  Ji Yoon Han; Joonhong Park
Journal:  Genes (Basel)       Date:  2021-09-07       Impact factor: 4.096

  2 in total

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