Complementary duplication and deletion of 17 (pcen→p11.2): A family with a supernumerary chromosome comprised of an interstitially deleted segment
- 1 September 1992
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 44 (1) , 37-40
- https://doi.org/10.1002/ajmg.1320440109
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangement.Molecular and Cellular Biology, 1990
- Formation of a minichromosome by excision of the proximal region of 17q in a patient with von Recklinghausen neurofibromatosisCytogenetic and Genome Research, 1990
- Human telomeres: fusion and interstitial sitesTrends in Genetics, 1989
- Interstitial deletion of (17)(p11.2p11.2) in nine patientsAmerican Journal of Medical Genetics, 1986
- De novo partial duplication of 17p [dup(17)(p12→p11.2)]: Clinical reportAmerican Journal of Medical Genetics, 1986
- Forty four probands with an additional ?marker? chromosomeHuman Genetics, 1985
- De novo tandem duplication 17p11->cenJournal of Medical Genetics, 1983
- Miller-Dieker syndrome: Lissencephaly andmonosomy 17pThe Journal of Pediatrics, 1983
- Duplication (17p) in a child with an isodicentric (17p) chromosomeAmerican Journal of Medical Genetics, 1983
- The dup(17p) syndromeAmerican Journal of Medical Genetics, 1982