Literature DB >> 7152517

Bisatellited dicentric chromosome: a report on a case with karyotype 47,XY, + psu dic(22)t(22;22)(22pter to cen to 22q11::22q11 to 22pter).

G Weilong, Y Aide, F Hongbao, L Shumou, Y Ju.   

Abstract

A 12-year-old boy with mental retardation and congenital anomalies was found to have a supernumerary small marker chromosome. This marker chromosome was proved to be bisatellited and dicentric by G-, C-, R-banding and the silverstaining technique.

Entities:  

Mesh：

Year:  1982        PMID： 7152517     DOI： 10.1007/bf00276596

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  6 in total

1.  Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother.

Authors:  J M Berg; H A Gardner; R J Gardner; E G Goh; V D Markovic; N E Simpson; R G Worton
Journal:  J Med Genet       Date:  1980-04       Impact factor: 6.318

2.  Trisomy 22 syndrome in a 26-year-old female--A follow-up examination.

Authors:  G Annerén; K H Gustavson
Journal:  Hereditas       Date:  1981       Impact factor: 3.271

3.  A 13-year-old girl with karyotype 47, XX, +i (22) (qll).

Authors:  A Smith; I S Fraser; R P Shearman
Journal:  J Med Genet       Date:  1981-02       Impact factor: 6.318

4.  Supernumerary bisatellited chromosome in a family ascertained through a patient with Sturge-Weber syndrome.

Authors:  A C Gutierrez; F Salamanca; R Lisker; A Segovia
Journal:  Ann Genet       Date:  1975-03

5.  Further dicentric X isochromosomes and deletions, and a new structure i(X)(pter to q2102 to pter).

Authors:  A Daniel; T Saville; D B Southall
Journal:  J Med Genet       Date:  1979-08       Impact factor: 6.318

6.  Homodicentric chromosomes: a distinctive type of dicentric chromosome.

Authors:  B E Ward; C M Bradley; J B Cooper; A Robinson
Journal:  J Med Genet       Date:  1981-02       Impact factor: 6.318
  6 in total
  2 in total

1.  Mirror image duplications of chromosome 21. Three new cases and discussion of the mechanisms of origin.

Authors:  R A Pfeiffer; J Loidl
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

Review 2.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132
  2 in total

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