Literature DB >> 9298749

Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissues.

S Rudnik-Schöneborn1, R Schubert, F Majewski, F Haverkamp, G Schwanitz.   

Abstract

Partial trisomy 6p is regarded as a distinct phenotype with short stature, failure to thrive, facial dysmorphisms with blepharophimosis, mental retardation and other malformations. An 18-month-old girl with typical features of partial trisomy 6p showed a de novo unbalanced translocation resulting in partial trisomy 6p21 to pter and partial monosomy 18p11 to pter. The translocation was observed in all fibroblasts analyzed, but only in 6% of the peripheral lymphocytes.

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Year:  1997        PMID: 9298749     DOI: 10.1111/j.1399-0004.1997.tb02530.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  1 in total

1.  Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardation.

Authors:  K Poirier; J Abriol; I Souville; C Laroche-Raynaud; C Beldjord; B Gilbert; J Chelly; T Bienvenu
Journal:  Hum Genet       Date:  2005-10-28       Impact factor: 4.132

  1 in total

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