Cri du chat syndrome due to meiotic recombination in a pericentric inversion 5 carrier
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1992.tb03679.x/fullpdf
Reference9 articles.
1. G-band position effects on meiotic synapsis and crossing over;Ashley;Genetics,1988
2. Familial partial monosomy 5q and trisomy 5q; three cases due to paternal pericentric inversion 5 (pl51q333);Beemer;Clin Genet,1984
3. Correlation between chromosomal breakpoint positions and synaptic behaviour in human males heterozygous for a pericentric inversion;Perdigo;Hum Genet,1989
4. Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the “Cri du Chat” syndrome;Faed;Cytogenetics,1972
5. Pericentric inversions - problems and significance for clinical genetics;Kaiser;Hum Genet,1984
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1. Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: Association of extra copy ofMSX2with craniosynostosis;American Journal of Medical Genetics Part A;2009-07
2. Cytogenetic and molecular characterization of a three-generation family with chromosome 5p terminal deletion;Clinical Genetics;2008-04-09
3. del5p/dup5q in a ‘cri du chat’ patient without parental chromosomal rearrangement;American Journal of Medical Genetics Part A;2006
4. “Cri-du-chat” syndrome in a patient born to a mother with a paracentric inversion of chromosome 5q;Annales de Génétique;2003-10
5. Delineation of the dup5q phenotype by molecular cytogenetic analysis in a patient with dup5q/del 5p (cri du chat);American Journal of Medical Genetics;2002-02-28
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