نتایج جستجو برای: karyotyping

تعداد نتایج: 1991  

2008
G. Ducrozet F. Bonnefoy D. Le Touzé P. Ferrant

In the present paper we propose a method for studying extreme-wave appearance based on the HigherOrder Spectral (HOS) technique proposed by West et al. (1987) and Dommermuth and Yue (1987). The enhanced HOS model we use is presented and validated on test cases. Investigations of freak-wave events appearing within longtime evolutions of 2-D and 3-D wavefields in open seas are then realized, and ...

G.L. Hwang, H. Farahmand, M.A Rahman, N. Maclean, S.H. Abdul Razak,

The induction of tetraploidy by means of cold, heat and multiple heat shock treatments was investigated on male fish from a growth-enhanced transgenic tilapia C118 line, crossed with wild type females. After the development a new multiple heat shock protocol (two heat treatments at 41oC in 60 and 80 min. after fertilization for 5 min. per each), chromosome and X-gal in situ staining assays demo...

2014
V. K. Govindan

Chromosome analysis is one of the most essential tasks in clinical research of cell genetics and genetic disease diagnosis. Automatic analysis of chromosomes by computers is very useful but there are many issues yet to address. Karyotyping identifies and displays chromosomes in a standard format. In this paper, a tool has been introduced that identifies abnormal chromosomes. The tool is able to...

2014
Kyoung-Bo Kim Jung-Sook Ha So-Jin Shin Chun Soo Kim Jin-Gon Bae

We report a case of de novo 7q interstitial deletion detected by conventional karyotyping and by microarray of amniotic fluid sampled during the prenatal period. A 32-year-old pregnant woman was evaluated at our hospital following detection of increased nuchal translucency at 12 weeks and 5 days of gestation. Conventional karyotyping revealed 46,XX,del(7)(q21q22) in 20 interphase mitotic cells,...

Journal: :British medical journal 1981
C Gosden K Buckton Z Fotheringham D J Brock

Prenatal karyotyping was undertaken in 569 consecutive amniotic fluid samples where the indication for amniocentesis was two sequential raised maternal serum alpha-fetoprotein concentrations. In 475 successful cultures five chromosome abnormalities were found--four constitutional anomalies (47,XXY; 47,XYY; an inherited inv(8) (p23q11); and a de-novo translocation t(6;7) (p11;p22) and a culture-...

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