Cytogenetic analyses on patients with Crouzon's and Apert's syndromes
Open Access
- 14 February 2008
- journal article
- case report
- Published by Springer Nature in Hereditas
- Vol. 105 (1) , 157-159
- https://doi.org/10.1111/j.1601-5223.1986.tb00653.x
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Interstitial deletion for a region in the long arm of chromosome 16Human Genetics, 1983
- Loss of the Y chromosome in a cultured human salivary‐gland adenocarcinomaJournal of Oral Pathology & Medicine, 1983
- Prenatal fetoscopic diagnosis of the Apert syndromeAmerican Journal of Medical Genetics, 1982
- Terminal 7p deletion and 1;7 translocation associated with craniosynostosisHuman Genetics, 1979
- Chromosome 7 short arm deletion and craniosynostosis a 7p-syndromeHuman Genetics, 1976