Intrachromosomal insertion of chromosome 7
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1992.tb03402.x/fullpdf
Reference32 articles.
1. Duplication 9q34 syndrome;Allderdice;Am J Hum Genet,1983
2. Familial mental retardation in a family with an inherited chromosome rearrangement;Chudley;J Med Genet,1974
3. Duplication of 16p from insertion of 16p into 16q with subsequent duplication due to crossing over within the inserted segment;Cohen;Am J Med Genet,1983
4. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories;Daniel;Am J Med Genet,1989
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1. Two familial intrachromosomal insertions with maternal dup(6)(p22.3p25.3) or dup(2)(q24.2q32.1) in recombinant offspring;Clinical Dysmorphology;2017-10
2. PGD for a carrier of an intrachromosomal insertion using aCGH;Systems Biology in Reproductive Medicine;2014-09-23
3. Duplication of intrachromosomal insertion segments 4q32→q35 confirmed by comparative genomic hybridization and fluorescentin situhybridization;Clinical and Experimental Reproductive Medicine;2011
4. Chromosome 6 between-arm intrachromosomal insertion with intrasegmental double inversion: A four-break model;American Journal of Medical Genetics Part A;2009-12-23
5. Chromosomal abnormalities and polymorphic variants in couples with repeated miscarriage in Mexico;Reproductive BioMedicine Online;2009-01
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