Abnormalities resulting from a familial pericentric inversion of chromosome 18
- 23 April 2008
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 14 (2) , 98-104
- https://doi.org/10.1111/j.1399-0004.1978.tb02113.x
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriersClinical Genetics, 2008
- Risk for recombinants in pericentric inversions of the (p11?q21) region of chromosome 18Human Genetics, 1977
- Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18.Journal of Medical Genetics, 1976
- Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18.Journal of Medical Genetics, 1976
- Trisomy for the distal half of the long arm of chromosome No. 18: A report of two affected sibsThe Journal of Pediatrics, 1974