Interstitial deletion of the long arm of chromosome 11 determined by fluorescencein situ hybridization
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical)
Link
http://www.nature.com/articles/jhg199314.pdf
Reference19 articles.
1. Bateman JB, Maumenee IH, Sparkes RS (1984): Peter's anomaly associated with partial deletion of the long arm of chromosome 11. Am J Ophthalmol97:11–15
2. Carnevale A, Blanco B, Grether P, Castillejos AR (1987): Interstitial deletion of the long arm of chromosome 11. Ann Genet30: 56–58
3. Fryns JP, Kleczkowska A, Buttiens M, Marien P, Van den Berghe H (1986): Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1. Clin Genet30: 255–260
4. Hori T, Takahashi E, Ayusawa D, Takeishi K, Kaneda S, Seno T (1990): Regional assignment of the human thymidylate synthase (TS) gene to chromosome band 18p11.32 by nonisotopicin situ hybridization. Hum Genet85: 576–580
5. Hori T, Takahashi E, Tanigami A, Tokino T, Nakamura Y (1992): A high-resolution cytogenetic map of 168 cosmid DNA markers for human chromosome 11. Genomics13: 129–133
Cited by 2 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. Partial monosomy of 11q22.2q22.3 including theSDHDgene in individuals with developmental delay;American Journal of Medical Genetics Part A;2015-03-03
2. Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report;Molecular Cytogenetics;2011-08-22
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