Bloom's syndrome in two Dutch families
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1977.tb00907.x/fullpdf
Reference21 articles.
1. Microtechnique for culturing leukocytes from whole blood;Arakaki;Cytogenetics,1963
2. Chromatid interchanges in ataxia telangiectasia, Bloom syndrome, Werner syndrome, and xeroderma pigmentosum;Bartram;Ann. hum. Genet. (Lond.),1976
3. The syndrome of congenital telangiectatic erythema and stunted growth;Bloom;J. Pediat.,1966
4. Bloom's syndrome: a probable new case with cytogenetic findings;Bourgeois;J. med. Genet.,1975
5. A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes;Chaganti;Proc. nat. Acad. Sci. (Wash.),1974
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1. Heterozygous manifestations in four autosomal recessive human cancer-prone syndromes: ataxia telangiectasia, xeroderma pigmentosum, Fanconi anemia, and Bloom syndrome;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;1992-12
2. Transition of Phenotypic Dimorphism with Regard to Spontaneous Sister Chromatid Exchange in Epstein-Barr Virus-transformed Bloom's Syndrome Lymphoblastoid Cell Lines;Japanese Journal of Cancer Research;1992-07
3. A catalogue of multiple congenital anomaly syndromes;Multiple Congenital Anomalies;1991
4. Chromosomal Instability Syndromes in Man;Advances in Mutagenesis Research;1991
5. Chromosome Instability Syndromes;Advances in Human Genetics;1989
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