Distribution of autosomal fragile sites in specimens cultured for prenatal fragile X diagnosis
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference33 articles.
1. Report of the committee on chromosome rearrangements in neoplasia and on fragile sites
2. Variation in the expression of aphidicolin-induced fragile sites in human lymphocyte cultures
3. Clinical implications and classification of the constitutive fragile sites
4. Constitutive fragile sites 1p31, 3p14, 6q26, and 16q23 and their use as controls for false-negative results with the fragile(X)
Cited by 4 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. Fragile sites, chromosomal lesions, tandem repeats, and disease;Frontiers in Genetics;2022-11-17
2. De novo and complex imbalanced chromosomal rearrangements revealed by array CGH in a patient with an abnormal phenotype and apparently “balanced” paracentric inversion of 14(q21q23);American Journal of Medical Genetics Part A;2008-08-01
3. Literaturverzeichnis;Manual der fetalen Medizin;1994
4. Fra(X)(q27.2), the common fragile site, observed in only one of 760 cases studied for the fragile X syndrome;American Journal of Medical Genetics;1992-04-15
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