Identification of a marker chromosome as inv dup(15) by molecular analysis
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1991.tb03083.x/fullpdf
Reference9 articles.
1. Forty-four probands with an additional “marker” chromosome;Buckton;Hum. Genet.,1985
2. Report of the committee on the genetic constitution of chromosomes 14 and 15;Cox;Cytogenet. Cell. Genet.,1989
3. Localization of the human prealbumin gene to 18p11.1-q12.3 by gene dose effect study of Southern blot hybridization;Jinno;Jpn. J. Hum. Genet.,1986
4. Origin of the extra chromosome in trisomy 18. A study of five patients using a restriction fragment length polymorphism;Kondoh;Hum. Genet.,1988
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1. Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype;Molecular Cytogenetics;2015-06-25
2. Complex small supernumerary marker chromosome with a 15q/16p duplication: clinical implications;Molecular Cytogenetics;2014-04-24
3. Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the mother;European Journal of Paediatric Neurology;2011-05
4. Developments in Molecular Genetic Diagnostics: An Update for the Pediatric Epilepsy Specialist;Pediatric Neurology;2011-05
5. A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomes;Clinical Genetics;2008-06-28
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