研究论文
Identification and characterization of normal length nonfluorescent Y chromosomes: cytogenetic analysis, Southern hybridization and non-isotopic in situ hybridization
Frank Speleman, Bart Van Der Auwera, Kathelijne Mangelschots, Miet Vercruyssen, Ton Raap, J. Wiegant, Margarita Craen, Jules G. Leroy
Ghent University Hospital University of Antwerp Leiden University
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学术脉络
学科主题
生物医学Chromosomal and Genetic Variations
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities · Genomic variations and chromosomal abnormalities
参考文献 48
Localization of the restriction fragment length polymorphism D14S1 (pAW-101) to chromosome 14q32.1 leads to 32.2 by in situ hybridization.
被引 38Tim Donlon, M. Litt, Samuel R. Newcom · PubMed · 1983
Giemsa-11 technique elucidating three structurally altered nonfluorescent Y chromosomes: r (Y), idic (Yp), dir tan dup (Yp).
被引 8G. Kosztolányi · PubMed · 1988
A DNA probe detecting multiple haplotypes of the human Y chromosome.
被引 113K Y Ngo, Gilles Vergnaud, Christoffer Johnsson · PubMed · 1986
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引用本文 24
Phenotype/Karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases
被引 383Lillian Y. F. Hsu · American Journal of Medical Genetics · 1994
Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature
被引 162Cathy M. Tuck‐Müller, Harold Chen, Jos� E. Mart�nez · Human Genetics · 1995
Constitutional translocation t(1;17)(p36;q12–21) in a patient with neuroblastoma
被引 142Geneviève Laureys, Frank Speleman, Ghislain Opdenakker · Genes Chromosomes and Cancer · 1990
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