| Literature DB >> 9298749 |
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.Entities:
Mesh:
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