Prenatal diagnosis of a familial interchromosomal insertion of Y chromosome heterochromatin
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference26 articles.
1. Insertional translocations: Report of two new families and review of the literature
2. Molecular characterization of a Y;15 translocation segregating in a family
3. Familial mental retardation in a family with an inherited chromosome rearrangement
Cited by 5 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. References;Benign & Pathological Chromosomal Imbalances;2014
2. A New Multicolor Fluorescence In Situ Hybridization Probe Set Directed Against Human Heterochromatin;Journal of Histochemistry & Cytochemistry;2012-04-17
3. Additional dark G-band in the p-arm of chromosome 19 due to a paracentric inversion with a breakpoint in the pericentromeric heterochromatin;American Journal of Medical Genetics;2001
4. Interchromosomal insertions;Human Genetics;2000-12-01
5. Prenatal diagnosis and outcome of mosaicism for ade novo unbalanced translocation identified in amniocytes;Prenatal Diagnosis;1998-08
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