Literature DB >> 535886

Pure trisomy 17p in 60% cells.

F Shabtai, A Shalev, J Chemke, I Halbrecht, E Elian.   

Abstract

A patient with pure trisomy of the short arm of chromosome 17 in 60% of the examined cells is reported. She presented a variant chromosome 1 with partial pericentric inversion and increased centromeric heterochromatin in one chromosome 17. The cytogenetic findings are discussed. The clinical findings are compared to those found in other reported cases of partial trisomy 17 and a delineation of a pure trisomy 17p attempted.

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Year:  1979        PMID: 535886     DOI: 10.1007/BF00278675

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


  12 in total

1.  Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors:  P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal:  Exp Cell Res       Date:  1960-09       Impact factor: 3.905

2.  An extra small metacentric chromosome identified as a deleted chromosome no. 17.

Authors:  W Palutke; H Chen; P Woolley; C Espiritu; H L Vogel; N Gohle; M Tyrkus
Journal:  Clin Genet       Date:  1976-05       Impact factor: 4.438

3.  Trisomy of the short arm of chromosome 17.

Authors:  E Latta; J J Hoo
Journal:  Humangenetik       Date:  1974

4.  Letter: Trisomy in abortion material.

Authors:  T Kajii; N Niikawa; A Ferrier; H Takahara
Journal:  Lancet       Date:  1973-11-24       Impact factor: 79.321

5.  A simple technique for demonstrating centromeric heterochromatin.

Authors:  A T Sumner
Journal:  Exp Cell Res       Date:  1972-11       Impact factor: 3.905

6.  Genotype and phenotype in human chromosome aberrations and in the minute mutants of Drosophila melanogaster.

Authors:  F Vogel
Journal:  Humangenetik       Date:  1973

7.  Trisomy 17 in two abortuses.

Authors:  K Ohama; I Kusumi; T Ihara
Journal:  Jinrui Idengaku Zasshi       Date:  1977-03

8.  Identification of isochromosome 17 in a girl with mental retardation and congenital malformations.

Authors:  F Salamanca-Gómez; S Armendares
Journal:  Ann Genet       Date:  1975-12

9.  Risk of malignancy and chromosomal polymorphism: a possible mechanism of association.

Authors:  F Shabtai; I Halbrecht
Journal:  Clin Genet       Date:  1979-01       Impact factor: 4.438

10.  Mapping of human chromosomal regions related to neoplasia: evidence from chromosomes 1 and 17.

Authors:  J D Rowley
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

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  2 in total

1.  De novo tandem duplication 17p11 leads to cen.

Authors:  Z Docherty; M A Hultén; M M Honeyman
Journal:  J Med Genet       Date:  1983-04       Impact factor: 6.318

2.  A molecular, cytogenetic, and clinical evaluation of mosaic tandem duplication 17p and Charcot-Marie-Tooth type 1A neuropathy.

Authors:  K S Reddy; M B Larsen
Journal:  J Med Genet       Date:  1998-02       Impact factor: 6.318

  2 in total

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