نتایج جستجو برای: xmni

تعداد نتایج: 97  

Journal: :Nucleic acids research 1988
R Shiang J C Murray J Wiggs T Dryja

SOURCE/DESCRIPTION: Probe D95HS0.5 is a 0.6 kb fragment subcloned into Blue-scribe a pUCl9 derivative from a bacterio phage library isolated by a cDNA probe of the retinoblastoma gene 1. The fragment is released with the enzymes Hindlll and Sail. POLYMORPHISMS: TaqI identifies a 2 allele polymorphism with a band at 2.1 kb and 1.8 kb with a frequency of 0.97 and 0.03 respectively. There are no c...

Journal: :Journal of medical genetics 1991
N S Van-de-Water D Ridgway P A Ockelford

New Zealand Maoris (72 X chromosomes) have been compared with Pacific Island Polynesians (121 X chromosomes) and Caucasian New Zealanders (51 X chromosomes) as a control group to determine the allelic frequency of six RFLPs associated with the genes for two X linked diseases (haemophilia A and haemophilia B). RFLPs examined were BclI, XbaI, and BglI within the factor VIII gene, the factor VIII ...

Journal: :Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 1999
A W Hilsdorf J E Krieger

Restriction fragment length polymorphism (RFLP) was used to examine the extent of mtDNA polymorphism among six strains of rats (Rattus norvegicus)--Wistar, Wistar Munich, Brown Norway, Wistar Kyoto, SHR and SHR-SP. A survey of 26 restriction enzymes has revealed a low level of genetic divergence among strains. The sites of cleavage by EcoRI, NcoI and XmnI were shown to be polymorphic. The use o...

Journal: :iranian journal of basic medical sciences 0
tahereh moradi division of genetics, department of biology, faculty of science, university of isfahan, isfahan, iran reihaneh vallian molecular genetics department, isfahan medical genetics center, isfahan, iran zahra fazeli department of genetics, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran asieh haghighatnia molecular genetics department, isfahan medical genetics center, isfahan, iran sadeq vallian division of genetics, department of biology, faculty of science, university of isfahan, isfahan, iran molecular genetics department, isfahan medical genetics center, isfahan, iran

objective(s): iran is considered as one of the high-prevalence areas for β-thalassemia with a rate of about 10% carrier frequency. molecular diagnosis of the disease is performed both by direct sequencing and indirectly by the use of polymorphic markers present in the beta globin gene cluster. however, to date there is no reliable information on the application of the markers in the iranian pop...

Background: Beta-thalassemia intermedia (BTI) is a type of hemoglobinopathy with an increased risk of cerebrovascular accidents, and transcranial cerebral Doppler ultrasonography (TCD) through determining the mean cerebral blood flow velocity (CBFV) can serve to predict the risk of a developing stroke. This study aims to compare patients with beta-thalassemia intermedia and healthy individuals ...

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