Literature DB >> 6968535

Hereditary 3;6 translocation : three cases of multiple malformations with partial trisomy 6p21 leads to pter.

L Pagano, G Fioretti, M Vetrella, E Risolo, C Casullo, A Celona, S Renda, A Rinaldi, V Ventruto.   

Abstract

The authors report on a family with a t(3;6). All four members of a sibship were carriers of the balanced translocation and two have had children with multiple malformations. The proband, six months old, had the karyotype 46,XY, t(3;6) (p26;p21) der pat. His clinical features were typical of the trisomy 6p syndrome. HLA typing data failed demonstrate both paternal haplotypes in the propositus.

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Year:  1980        PMID: 6968535

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  2 in total

1.  Duplication 6p and deletion 9p.

Authors:  C Lytle; J Wade; A Farrier; F Flohrschutz; B Hecht; J Allanson
Journal:  J Med Genet       Date:  1989-01       Impact factor: 6.318

2.  Genetic mapping: chromosomes 6-22.

Authors:  B Keats
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025

  2 in total

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