Literature DB >> 13889990

An aberrant small acrocentric chromosome.

J R ELLIS, R MARSHALL, L S PENROSE.   

Abstract

Keywords:  CHROMOSOMES

Mesh：

Year:  1962        PMID： 13889990     DOI： 10.1111/j.1469-1809.1962.tb01312.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN： 0003-4800            Impact factor:   1.670


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  11 in total

1.  A PROBABLE CASE OF INCOMPLETE TRISOMY OF A CHROMOSOME OF THE 13-15 GROUP.

Authors:  J ISHMAEL; K M LAURENCE
Journal:  J Med Genet       Date:  1965-06       Impact factor: 6.318

2.  A familial minute isochromosome.

Authors:  D Mukerjee; W J Burdette
Journal:  Am J Hum Genet       Date:  1966-01       Impact factor: 11.025

3.  A further example of familial Gp+ associated with trisomy G.

Authors:  I Subrt
Journal:  Humangenetik       Date:  1970

4.  Inherited pericentric inversion of chromosome no. 4.

Authors:  M G Wilson; J W Towner; G S Coffin; I Forsman
Journal:  Am J Hum Genet       Date:  1970-11       Impact factor: 11.025

5.  A masculinizing syndrome associated with a doubly-satellited extra chromosome.

Authors:  R A Rohde
Journal:  J Med Genet       Date:  1965-12       Impact factor: 6.318

6.  Presumed disturbance of a nucleolus organizer in man: chromosome 13qs and monosomy 15 mosaicism.

Authors:  H Hoehn; H Reinwein
Journal:  Humangenetik       Date:  1971

7.  The genetic significance of accessory bisatellited marker chromosomes.

Authors:  P Steinbach; M Djalali; I Hansmann; E Kattner; M Meisel-Stosiek; H D Probeck; A Schmidt; M Wolf
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

Review 8.  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

Review 9.  [Cat-eye syndrome. Clinical and cytogenetical differentialdiagnosis (author's transl)].

Authors:  J Kunze; M Tolksdorf; H R Wiedemann
Journal:  Humangenetik       Date:  1975

10.  A case of extra small acrocentric bisatellited chromosome in a non mongoloid child.

Authors:  M Furbetta; G Rosi; M Biagioni; P Cossu; A Cao
Journal:  Humangenetik       Date:  1975-09-20
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