Meiotic analysis by FISH of a human male 46,XY,t(15;20)(q11.2;q11.2) translocation heterozygote: quadrivalent configuration, orientation and first meiotic segregation

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

D. Pinkel, J. E. Landegent, Colin C. Collins et al. · Proceedings of the National Academy of Sciences · 1988 · 1.3K citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome

Robert D. Nicholls, Joan H.M. Knoll, Merlin G. Butler et al. · Nature · 1989 · 887 citations

Life Sciences, Genetics, Molecular Genetics +11

Uniparental paternal disomy in Angelman's syndrome

S Malcolm, Jill Clayton‐Smith, M. Nichols et al. · The Lancet · 1991 · 330 citations

Life Sciences, Genetics, Cytogenetics +6

Chiasma distribution at diakinesis in the normal human male

Maj Hultén · Hereditas · 2009 · 291 citations · Full text

Life Sciences, Biology, Genetics +14

Cytogenetic Analysis by In Situ Hybridization with Fluorescently Labeled Nucleic Acid Probes

Daniel Pinkel, Joe W. Gray, B. J. Trask et al. · Cold Spring Harbor Symposia on Quantitative Biology · 1986 · 286 citations

Life Sciences, Genetics, Cytogenetics +15