A case of de novo trisomy 12p syndrome
- 28 June 2008
- journal article
- case report
- Published by Wiley in Clinical Genetics
- Vol. 35 (5) , 382-386
- https://doi.org/10.1111/j.1399-0004.1989.tb02958.x
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Centric fission, centromere‐telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomyClinical Genetics, 1987
- New chromosomal dysmorphic syndromesEuropean Journal of Pediatrics, 1981
- Trisomy 12p syndromeHuman Genetics, 1979
- Two cases of trisomy 12p due to rcpt(12;21)(p11;p11) inherited through three generationsHuman Genetics, 1979
- Double translocation t(7;12),t(2;6) heterozygosity in one familyHuman Genetics, 1978
- Identification of partial 12 trisomy by quinacrine fluorescenceThe Journal of Pediatrics, 1973