18p? Syndrome: an unusual case and diagnosis by in situ hybridization with chromosome 18-specific alphoid DNA sequence
- 1 February 1986
- journal article
- case report
- Published by Springer Nature in Human Genetics
- Vol. 72 (2) , 185-187
- https://doi.org/10.1007/bf00283945
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
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- A cloned repeated DNA sequence in human chromosome heteromorphismsCytogenetic and Genome Research, 1981
- The identification of a repeated DNA sequence involved in the karyotype polymorphism of the human Y chromosomeCytogenetic and Genome Research, 1978
- Chromosomal localisation of DNA sequences in condensed and dispersed human chromatinExperimental Cell Research, 1975