2021
DOI: 10.1186/s13039-021-00560-3
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Placing women in Cytogenetics: Lore Zech and the chromosome banding technique

Abstract: Background Scholars agree that Torbjörn Caspersson’s lab at the Institute of Medical Cell Research and Genetics at the Karolinska Institute, Sweden, played a key role in the first description of the so-called Q-banding technique. It laid the foundation for a new era of cytogenetic diagnostics and had a lasting impact in several areas of biology and medicine. Methods Based on a mixed-method approach, essential aspects of the history of human cytogen… Show more

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Cited by 2 publications
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“…Unequivocal identification of individual chromosomes and chromosomal regions became possible easier in the early 1970s with the development of several techniques to stain each chromosome with unique regional banding patterns that could be observed under a microscope. While many structural rearrangements had already been observed with solid staining of chromosomes, techniques such as Giemsa (G-banding) (Barcia, 2007) and quinacrine mustard (Q-banding) (Söhner and Hansson, 2021) allowed for easier interrogation of structural rearrangements, and led to the discovery of more subtle chromosome alterations. This also prompted the establishment of the International System for Human Cytogenetic Nomenclature (ICSN) in 1971, which enabled a standardized description of this chromosomal variation at different levels of resolution (Paris Conference (1971): Standardization in human cytogenetics., 1975).…”
Section: Chromosomes In Piecesmentioning
confidence: 99%
“…Unequivocal identification of individual chromosomes and chromosomal regions became possible easier in the early 1970s with the development of several techniques to stain each chromosome with unique regional banding patterns that could be observed under a microscope. While many structural rearrangements had already been observed with solid staining of chromosomes, techniques such as Giemsa (G-banding) (Barcia, 2007) and quinacrine mustard (Q-banding) (Söhner and Hansson, 2021) allowed for easier interrogation of structural rearrangements, and led to the discovery of more subtle chromosome alterations. This also prompted the establishment of the International System for Human Cytogenetic Nomenclature (ICSN) in 1971, which enabled a standardized description of this chromosomal variation at different levels of resolution (Paris Conference (1971): Standardization in human cytogenetics., 1975).…”
Section: Chromosomes In Piecesmentioning
confidence: 99%