Results 1 to 10 of about 100,385 (298)
Novel Insights into Normal Karyotype Miscarriage: Distinctive Patterns and Implications for Diagnosis Based on Next-Generation Sequencing Analysis. [PDF]
Reprod Med BiolKubota Y +5 more
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Some of the next articles are maybe not open access.
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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Cordocentesis for rapid karyotyping
American Journal of Obstetrics and Gynecology, 1990Pure fetal blood was obtained by cordocentesis in 101 fetuses of 96 patients at 15 to 38 weeks' gestation. Rapid karyotype was obtained within 2 to 4 days by fetal lymphocyte culture. Chromosomal abnormality was detected in 12 (11.9%) fetuses.
D M, Shah +4 more
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2011
Pulsed field gel electrophoresis enables separation of fungal chromosomes up to several megabases and is a worthwhile tool for fungal karyotyping. The germ tube burst method is a technique to separate fungal chromosomes of any size for chromosome number determination as well as in situ hybridization.
Mehrabi, R. +4 more
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Pulsed field gel electrophoresis enables separation of fungal chromosomes up to several megabases and is a worthwhile tool for fungal karyotyping. The germ tube burst method is a technique to separate fungal chromosomes of any size for chromosome number determination as well as in situ hybridization.
Mehrabi, R. +4 more
openaire +2 more sources