Literature DB >> 3585946

Duplication 9p due to unequal sister chromatid exchange.

T Mattina, G Sorge, G Milone, R Garozzo, L Conti.   

Abstract

A case of trisomy 9p syndrome is reported. The karyotype showed a tandem duplication of the short arm and of the inverted heterochromatic block of chromosome 9. Unequal sister chromatid exchange seems to be the only possible cause of this finding.

Entities:  

Mesh：

Year:  1987        PMID： 3585946      PMCID： PMC1050057          DOI： 10.1136/jmg.24.5.303

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


  4 in total

Review 1.  Genetics of the +p9 syndrome.

Authors:  I W Lurie; G I Lazjuk; D B Gurevich; S S Usoev
Journal:  Hum Genet       Date:  1976-04-15       Impact factor: 4.132

Review 2.  Partial trisomy 9 : clinical and cytogenetic correlations.

Authors:  C Baccichetti; E Lenzini; P Temperani; R Pallotta; P L Giorgi; E Tarantino; G Mengarda; B Dordi
Journal:  Ann Genet       Date:  1979

3.  Sequential staining of euchromatic and heterochromatic regions of the human Y chromosome.

Authors:  V J Goyanes
Journal:  J Med Genet       Date:  1980-12       Impact factor: 6.318

4.  De novo tandem duplication 9p (p12----p24) with normal GALT activity in red cells.

Authors:  T Motegi; K Watanabe; N Nakamura; T Hasegawa; Y Yanagawa
Journal:  J Med Genet       Date:  1985-02       Impact factor: 6.318
  4 in total
  4 in total

1.  Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).

Authors:  B R Haddad; A E Lin; H Wyandt; A Milunsky
Journal:  J Med Genet       Date:  1996-12       Impact factor: 6.318

2.  A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation.

Authors:  Khaled K Abu-Amero; Ali M Hellani; Mustafa A Salih; Mohammad Z Seidahmed; Tageldin S Elmalik; Ghassan Zidan; Thomas M Bosley
Journal:  BMC Med Genet       Date:  2010-09-21       Impact factor: 2.103

3.  Intrachromosomal tandem duplication and repeat expansion during attempts to inactivate the subtelomeric essential gene GSH1 in Leishmania.

Authors:  Angana Mukherjee; Lance D Langston; Marc Ouellette
Journal:  Nucleic Acids Res       Date:  2011-06-21       Impact factor: 16.971

4.  Cytogenetic and array-CGH characterization of a complex de novo rearrangement involving duplication and deletion of 9p and clinical findings in a 4-month-old female.

Authors:  P J Hulick; K M Noonan; S Kulkarni; D J Donovan; M Listewnik; C Ihm; J M Stoler; S Weremowicz
Journal:  Cytogenet Genome Res       Date:  2010-01-06       Impact factor: 1.636
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.