Results 351 to 360 of about 140,678 (408)
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Mammalian karyotype evolution

Nature Reviews Genetics, 2007
The chromosome complements (karyotypes) of animals display a great diversity in number and morphology. Against this background, the genomes of all species are remarkably conserved, not only in transcribed sequences, but also in some chromosome-specific non-coding sequences and in gene order.
Malcolm A. Ferguson-Smith   +1 more
openaire   +3 more sources

An infant with an XXXYY karyotype

Clinical Genetics, 1974
An 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 non‐fluorescent. An attempt was made to find the origin of the extra X chromosomes by testing the Xg blood group in the whole ...
E. M. E. Smit   +4 more
openaire   +3 more sources

Constitutional karyotypes in retinoblastoma

Ophthalmic Paediatrics and Genetics, 1987
The 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 ...
J de Grouchy, Catherine Turleau
openaire   +2 more sources

Multicolour karyotyping

The Lancet, 2001
38 Jarraud S, Peyrat MA, Lim A, et al. egc, a highly prevalent operon of enterotoxin gene, forms a putative nursery of superantigens in Staphylococcus aureus. J Immunol 2001; 166: 669–77. 39 Reed SB, Wesson CA, Liou LE, et al. Molecular characterization of a novel Staphylococcus aureus serine protease operon. Infect Immun 2001; 69: 1521–27. 40 Naito T,
Lee, C   +6 more
openaire   +3 more sources

Cordocentesis for rapid karyotyping

American Journal of Obstetrics and Gynecology, 1990
Pure 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.
Dinesh M. Shah   +4 more
openaire   +2 more sources

Efficient karyotyping of metaphase chromosomes using incremental learning

, 2013
Automated karyotyping for chromosome classification is an essential task in cytogenetics for diagnosis of genetic disorders and has therefore been an important pattern recognition problem. The existing learning approaches generally discard the previously
P. Joshi   +3 more
semanticscholar   +1 more source

Single-nucleotide polymorphism array karyotyping in clinical practice: where, when, and how?

Seminars in Oncology, 2012
Single-nucleotide polymorphism array (SNP-A) karyotyping is a new technology that has enabled genome-wide detection of genetic lesions in human cancers, including hematopoietic neoplasms.
A. Sato-Otsubo, M. Sanada, S. Ogawa
semanticscholar   +1 more source

Karyotype is not dead (yet)!

European Journal of Medical Genetics, 2016
While array-comparative genomic hybridization (a-CGH) and next-generation sequencing (NGS or exome) technologies have swiftly spread throughout the medical field, karyotype has gradually lost its leading role among genetic tests. Several international guidelines recommend starting with a-CGH screening then going on with exome analysis when ...
Pasquier, Laurent   +13 more
openaire   +4 more sources

Heterochromatin, colchicine, and karyotype

Chromosoma, 1965
Species of Chilocorus differ in chromosome number owing to centric fusion of metacentric chromosomes. The concomitant loss of arms is tolerated because in all unfused chromosomes one arm is completely heterochromatic, the other euchromatic. Under the influence of colchicine, the arms of unfused and fused chromosomes contract differentially.
openaire   +3 more sources

A database of amphibian karyotypes

Chromosome Research, 2019
One of the first characteristics that we learn about the genome of many species is the number of chromosomes it is divided among. Despite this, many questions regarding the evolution of chromosome number remain unanswered. Testing hypotheses of chromosome number evolution using comparative approaches requires trait data to be readily accessible and ...
Riddhi D. Perkins   +6 more
openaire   +3 more sources

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