نتایج جستجو برای: inheritance and pathogenecity

تعداد نتایج: 16831145  

Mahnaz Khattak, Salahuddin Salahuddin, Shuhrat Shah,

A new test of inheritance, S, is proposed, which uses information from affected as well as unaffected siblings in the fam­ ily. The siblings are analyzed in terms of similarities of haplotypes. The distribution of the proposed S­test is derived under the null hypothesis of random inheritance. Mean and variance are obtained for the distribution. The test is then applied to data sets publ...

Journal: :iranian journal of child neurology 0
massoud houshmand national institute for genetic engineering and biotechnology (nigeb), tehran, iran

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The dissolution of the Western-dominated Postwar Order, and the Eurocentric myths that sustain it, presents a unique opportunity to ponder an old question posed by every new generation: How can philosophy, which Islamic and ancient Greek learning traditions have long defined as the pursuit of “wisdom,” resume its millennial civilizing role? This paper looks beyond passing political events to re...

Background and Aims: Retinitis pigmentosa (RP) is the most common form of inherited retinal degeneration, photoreceptors loss of which in the retina causes visual loss. The purpose of the present study was to determine patterns of inheritance in RP patients in Yazd to help the health professional for designing suitable laboratory testing for the high risk families. Materials and Methods: Thirt...

برهانی, دکتر مرتضی, کوهساری , دکتر محمدرضا ,

ABSTRACT: DRASH Syndrome is a rare congenital disorder,and the triad of drash syndrome are progressive renal insufficiency ,male pseudohermaphroditism & Wilms tumor .All of the reported cases were sporadic and autosomal dominant inheritance was suspected in some references. We diagnosed a 32- month child with this syndrome in IRAN in 1993. He was presented with wilms tumor and also had male p...

Journal: :acta medica iranica 0
saeid morowati research center for human genetics, baqiyatallah university of medical sciences, tehran, iran. mobin yasini2 research center of molecular biology, baqiyatallah university of medical sciences, tehran, iran. reza ranjbar research center of molecular biology, baqiyatallah university of medical sciences, tehran, iran. ali asghar peivandi faculty of medicine, shahid beheshti university of medical sciences, tehran, iran. mohsen ghadami medical genetics department, faculty of medicine, tehran university of medical sciences, tehran, iran.

ankyloglossia (tongue-tie) is a congenital anomaly with a prevalence of 4-5% and characterized by an abnormally short lingual frenulum. for unknown reasons the abnormality seems to be more common in males. the pathogenesis of ankyloglossia is not known. the authors report a family with isolated ankyloglossia inherited as an autosomal dominant or recessive trait. the identification of the defect...

Journal: :School Science and Mathematics 1917

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