Interstitial deletion of chromosome 21
- 23 April 2008
- journal article
- case report
- Published by Wiley in Clinical Genetics
- Vol. 22 (4) , 215-219
- https://doi.org/10.1111/j.1399-0004.1982.tb01436.x
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Partial trisomy 21Clinical Genetics, 1980
- Normal phenotype and partial trisomy for the G positive region of chromosome 21.Journal of Medical Genetics, 1979
- Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21)Human Genetics, 1979
- De novo simultaneous reciprocal translocation and deletion.Journal of Medical Genetics, 1978
- Full monosomy 21: A clinically recognizable syndrome?Human Genetics, 1977
- Clinical and cytogenetic studies of two infants with partial monosomy GHuman Genetics, 1977
- Karyotype 45,XX,-21/46,XX,21q- in an infant with symptoms of G-deletion syndrome IJournal of Medical Genetics, 1974
- A Case of a Girl with a 21 Ring ChromosomeHuman Heredity, 1974
- Identification of 21 r and 22r chromosomes by quinacrine fluorescenceClinical Genetics, 1972
- New Technique for Distinguishing between Human ChromosomesNature New Biology, 1971