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Current Protocols in Human Genetics, 1998
AbstractRelevant portions of the new International System for Human Cytogenetic Nomenclature (ISCN 1995) have been reproduced in this appendix (with permission from Karger, the original publisher). The new rules supersede all previous rules and include guidelines for cancer cytogenetics as well as new recommendations for nomenclature when in situ ...
R R, Schreck, C, Distèche
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AbstractRelevant portions of the new International System for Human Cytogenetic Nomenclature (ISCN 1995) have been reproduced in this appendix (with permission from Karger, the original publisher). The new rules supersede all previous rules and include guidelines for cancer cytogenetics as well as new recommendations for nomenclature when in situ ...
R R, Schreck, C, Distèche
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Is Karyotyping Couples Experiencing Recurrent Miscarriage Worth the Cost?
BJOG: an International Journal of Obstetrics and Gynaecology, 2010 Karyotyping couples that have had recurrent miscarriages detects balanced rearrangements in carrier parents who can be offered prenatal cytogenetic analysis to prevent the birth of a subsequent child with an unbalanced rearrangement.
Grant, E. +5 more
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Nature Protocols, 2007
Detection of copy number variation in the human genome is important for identifying naturally occurring copy number polymorphisms as well as alterations that underlie various human diseases, including cancer. Digital karyotyping uses short sequence tags derived from specific genomic loci to provide a quantitative and high-resolution view of copy number
Rebecca J, Leary +3 more
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Detection of copy number variation in the human genome is important for identifying naturally occurring copy number polymorphisms as well as alterations that underlie various human diseases, including cancer. Digital karyotyping uses short sequence tags derived from specific genomic loci to provide a quantitative and high-resolution view of copy number
Rebecca J, Leary +3 more
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The karyotype of blastic crisis
Cancer Genetics and Cytogenetics, 1987The nonrandomness of chromosome clonal evolution in blastic crisis of chronic myeloid leukemia is well established, with three major changes [+8, +Ph, i(17q)] occurring alone or in combination in over 70% of the patients. The chromosome changes observed in different tissues may reveal the origin of the abnormal clones, as well as provide evidence for ...
ALIMENA, Giuliana +4 more
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Nature, 1964
THROUGH work with short-term cultures of leucocytes from peripheral blood according to the phytohaemagglutinin method, the opportunity arose to examine the chromosome complement of the red fox (Vulpes vulpes Lin.). As no description of the chromosome morphology has previously been published, these observations are of some interest.
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THROUGH work with short-term cultures of leucocytes from peripheral blood according to the phytohaemagglutinin method, the opportunity arose to examine the chromosome complement of the red fox (Vulpes vulpes Lin.). As no description of the chromosome morphology has previously been published, these observations are of some interest.
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Chromosoma, 1971
A denaturating and renaturating technique, applied to mouse chromosomes, makes visible characteristic banding patterns by which all elements of the karyotype can be individually distinguished. The Y chromosome as a whole appears darkly stained. The X chromosome comprises 6.33% of the homogametic haploid set.
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A denaturating and renaturating technique, applied to mouse chromosomes, makes visible characteristic banding patterns by which all elements of the karyotype can be individually distinguished. The Y chromosome as a whole appears darkly stained. The X chromosome comprises 6.33% of the homogametic haploid set.
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Karyotyping, Is It Worthwhile in Transsexualism?
Journal of Sexual Medicine, 2011 Introduction. Karyotyping is often performed in transsexual individuals. Aim. Quantification and characterization of karyotype findings and abnormalities in transsexual persons. Main Outcome Measures. Karyotypes were listed both in male-to-female and in
Björn Menten +2 more
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