نتایج جستجو برای: excess method average chromosome

تعداد نتایج: 2095877  

2016
Kajendralala Mitra

From the health officer's report for this period, it appears that the aggregate mortality of the months of July, August and September was greatly in excess of the average of the preceding decade. " Fever" continues to contribute a high figure. Cholera was decidedly below the average, bowel complaints slightly so, smallpox in decided excess but declining ; the figures for the three months being ...

Journal: :journal of sciences islamic republic of iran 0

down syndrome is one of the most common causes of mental retardation observed in approximately 1/700 live birth. the use of two or more str markers related to chromosome 21 facilitates the diagnosis of down syndrome within about six hours from the collection of the samples. this is the first study has been performed in iranian population to assess the diagnostic value of using small tandem repe...

Journal: :Clinical and experimental rheumatology 2005
L Eder M Rozenbaum N Boulman E Aayubkhanov E Wolfovitz D Zisman I Rosner

Only a limited number of cases of Behçet's disease and hematological malignancies have been reported in the literature. We report the case of a 45 year old female patient with Behçet's disease who developed myelodysplastic syndrome, refractory anemia with excess blasts in transformation subtype, with complex chromosomal abnormalities, including excess of chromosome 8, following several years of...

2013
Evan Koch Mickey Ristroph Mark Kirkpatrick

Long-range linkage disequilibria (LRLD) between sites that are widely separated on chromosomes may suggest that population admixture, epistatic selection, or other evolutionary forces are at work. We quantified patterns of LRLD on a chromosome-wide level in the YRI population of the HapMap dataset of single nucleotide polymorphisms (SNPs). We calculated the disequilibrium between all pairs of S...

Journal: :Molecular biology and evolution 2010
Richard P Meisel Benedict B Hilldorfer Jessica L Koch Steven Lockton Stephen W Schaeffer

Drosophila X chromosomes are disproportionate sources of duplicated genes, and these duplications are usually the result of retrotransposition of X-linked genes to the autosomes. The excess duplication is thought to be driven by natural selection for two reasons: X chromosomes are inactivated during spermatogenesis, and the derived copies of retroposed duplications tend to be testis expressed. ...

Journal: :iranian journal of analytical chemistry 2014
azar bagheri gh.

spectrophotometric and electrochemical studies were successfully used in quantitative analysis of amitriptyline hydrochloride (ath) and nortriptyline hydrochloride (nth). conductometric titration were carried out in equeous solution using iodide and dopamine and serotonine as titrant. two new methods using spectrophotometry are dascribed for the determination of (ath) and (nth) with potassium b...

Journal: :Blood 1986
C Mecucci A Van Orshoven G Tricot J L Michaux A Delannoy H Van den Berghe

We present four patients with acute nonlymphocytic leukemia, one M2 and three M4 French-American-British (FAB) types and one patient with refractory anemia with excess of blasts in transformation who at diagnosis had trisomy of chromosome 4 as the primary karyotypic anomaly. This chromosome anomaly probably defines a previously undescribed subset of acute nonlymphoid leukemias. Hematologic char...

Journal: :Pattern Recognition Letters 2006
Mehdi Moradi Seyed Kamaledin Setarehdan

Karyotyping, a standard method for presenting pictures of the human chromosomes for diagnostic purposes, is a long standing, yet common technique in cytogenetics. Automating the chromosome classification process is the first step in designing an automatic karyotyping system. The main aim in this study was to define a new group of features for better representation and classification of chromoso...

A. K. Esmailizadeh E. Nasirifar H. Moradian S. S. Sohrabi

The objective of this study was to identify the quantitative trait loci (QTL) affecting carcass traits on chromosome 1 in Japanese quail. The populations comprised of 422 progeny in 9 half-sib families. Phenotypic data on carcass weight, carcass parts, and the internal organs were collected on 422 progeny. Nine half-sib families were genotyped for 8 microsatellite markers covering chromosomes 1...

Journal: :American journal of medical genetics. Part A 2009
Tiffany Renee Oliver Archit Bhise Eleanor Feingold Stuart Tinker Nirupama Masse Stephanie L Sherman

Previous studies on relatively small samples of individuals with trisomy 21 caused by paternally derived errors have shown that: (1) advanced paternal age is not a risk factor for chromosome 21 nondisjunction (NDJ), (2) absence of recombination, but not the location of recombination is associated with paternal NDJ and (3) there is an excess of males among live-births with paternally derived tri...

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