Results 301 to 310 of about 162,657 (334)
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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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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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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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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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Embryonic karyotype in recurrent miscarriage with parental karyotypic aberrations
Fertility and Sterility, 2006To assesses chromosomal aberrations in the abortus in recurrent miscarriage, in the presence of parental chromosomal aberrations.Retrospective comparative cohort study.Tertiary referral unit in university hospital.One thousand one hundred eight patients with 3-16 miscarriages before 20 weeks gestation; 113 patients with and 995 without chromosomal ...
Howard, Carp +5 more
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Cell and Tissue Biology, 2017
In this paper, the protocol which we have developed to get satisfactory spreads of Amoeba proteus mitotic chromosomes is presented, and the process of karyotyping this amoeba species is described. This protocol allows obtaining of extended chromosomic with repeatable chromomeres pattern in individual chromosomes.
S Yu, Demin +4 more
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In this paper, the protocol which we have developed to get satisfactory spreads of Amoeba proteus mitotic chromosomes is presented, and the process of karyotyping this amoeba species is described. This protocol allows obtaining of extended chromosomic with repeatable chromomeres pattern in individual chromosomes.
S Yu, Demin +4 more
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An infant with an XXXYY karyotype
Clinical Genetics, 1974An infant with mild retardation of psychomotor development and ambiguous genitalia was found to have a 49, XXXYY karyotype. The identity of the chromosomes was established by different banding methods, both fluorescent and nonâfluorescent. An attempt was made to find the origin of the extra X chromosomes by testing the Xg blood group in the whole ...
F A, Lecluse-van der Bilt +4 more
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Constitutional karyotypes in retinoblastoma
Ophthalmic Paediatrics and Genetics, 1987The improvement of chromosome banding techniques has much increased the frequency of detected forms of retinoblastoma. Ten rearrangements involving 13q14 were observed in a series of 105 retinoblastoma patients including: five de novo deletions, one of them with suspected mosaicism; one de novo apparently balanced translocation; four deletions due to ...
C, Turleau, J, De Grouchy
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