Partial trisomy 13 presumably due to recombination in an inversion heterozygote and by unequal crossing-over
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.1978.tb01898.x/fullpdf
Reference22 articles.
1. Hemoglobin Cranston, an unstable variant having an elongated beta chain due to nonhomologous crossover between two normal beta chain genes.
2. Differential binding of alkylating fluorochromes in human chromosomes
3. Trisomy for the Distal Segment of Chromosome 13
4. Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals.
Cited by 18 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Novel case of paternal paracentric inversion causing partial trisomy 13 and review of the literature;American Journal of Medical Genetics Part A;2017-04-10
2. A recognizable phenotype in a child with partial duplication 13q in a family with t(10q;13q);Clinical Genetics;2008-04-23
3. Characterization of a familial balanced rec(13) in a child with mild MR and his half-sibling with two structurally rearranged chromosomes 13;American Journal of Medical Genetics Part A;2005
4. Boy with bilateral retinoblastoma due to an unusual ring chromosome 13 with activation of a latent centromere;American Journal of Medical Genetics;2001
5. De novo partial duplication of long arm of chromosome 13: dup(13)(q12?q14);American Journal of Medical Genetics;2000-06-05
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