نتایج جستجو برای: investigation of inheritance

تعداد نتایج: 21177419  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شهید چمران اهواز - دانشکده ادبیات و علوم انسانی 1394

پژوهش حاضر با پیوند رسانه های قدیمی و جدید یاد دهی و یادگیری _طرح داستان و بازی های همراه ــ در یک پو دمان ترکیبی، در صدد قیاس شیوه ی یاد دهی و یادگیری مبتنی بر بازی مهارت های فرعی و اصلی واژگان، خواندن و نوشتار سواد انگلیسی با شیوه های مرسوم آن بود. به این منظور با کاربرد یک طرح سه گانه همراه با الگوی نظام آموزشی (تومی، 2010)، بازی های از پیش ساخته شده و بومی قابل عرضه از طریق ارتباطات سیّار (ب...

2005
Daniel Chernuchin Oliver S. Lazar Gisbert Dittrich

This paper presents, explores and compares object-oriented approaches for roles in statically typed programming languages. We choose five solutions which support information hiding. On the one hand, we investigate the established object-oriented possibilities multiple and interface inheritance and the role object pattern, on the other hand, we examine the language extensions Object Teams and th...

Journal: : 2022

The article is devoted to clarifying the essence of phenomenon dormant inheritance in law. It has been concluded that right ownership inherited property acquired by heir retrospectively from time was opened, regardless legal regime property. However, until moment state registration ownership, limited his/her ability dispose real estate, particular alienating it. this limitation does not at all ...

2016
H. S. HAYRAPETYAN T. F. SARKISIAN S. A. ATOYAN

The aim of this study is the investigation of one mutation carriers of MEFV gene among Armenian population. We designed and established the genetic register for proper collection of patients’ data including their ethnicity, clinical and laboratory data, as well as family cases. According to the results the frequency of FMF inheritance with only one mutation of MEFV gene among Armenian populatio...

2012
Attila Szvetko Nicole Martin Chris Joy Andrea Hayward Bob Watson Andrew Cary Stephen Withers

We describe a familial pattern of gonosomal-autosomal translocation between the X and 18 chromosomes, balanced and unbalanced forms, in male and female siblings. The proposita was consulted for hypergonadotropic hypogonadism. Karyotype analysis revealed a balanced 46, X, t(X;18)(q22.3;q23) genotype. The sister of the proband presented with oligomenorrhea with irregular menses and possesses an u...

2012
Xingyuan Zhang Christian Urban Chunhan Wu

In real-time systems with threads, resource locking and priority scheduling, one faces the problem of Priority Inversion. This problem can make the behaviour of threads unpredictable and the resulting bugs can be hard to find. The Priority Inheritance Protocol is one solution implemented in many systems for solving this problem, but the correctness of this solution has never been formally verif...

Journal: :مدیریت خاک و تولید پایدار 0
فریده کریمی دهکردی فارغ التحصیل کارشناسی ارشد دانشگاه آزاد اسلامی خوراسگان واحد اصفهان احمد جلالیان استاد گروه خاک شناسی، ، دانشکده کشاورزی دانشگاه آزاد اسلامی واحد خوراسگان (اصفهان)، اصفهان عبدالمحمد محنت کش عضو هیات علمی مرکز تحقیقات کشاورزی و منابع طبیعی استان چهارمحال و بختیاری ناصر هنرجو استادیار گروه خاک شناسی، ، دانشکده کشاورزی دانشگاه آزاد اسلامی واحد خوراسگان (اصفهان)، اصفهان

this study was conducted to investigate the type and origin of clay minerals via several profiles in lordegan hilly lands. the profiles were located in two kinds of land uses including forest and dry farm at different slope positions as sampling sites. the soil saples were collected from two depths of soil horizons to indicate cec, soil texture, oc%, calcium carbonate equivalent, x-ray diffract...

Journal: :South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 2011
Ntobeko B A Ntusi Ambroise Wonkam Gasnat Shaboodien Motasim Badri Bongani M Mayosi

BACKGROUND Studies from Europe and North America suggest that 20 - 50% of patients with dilated cardiomyopathy (DCM) may have familial disease. There is little information on the frequency and clinical genetics of familial DCM in Africa. PURPOSE To determine the frequency and probable mode of inheritance of familial DCM in patients referred for investigation of the cause of DCM at a tertiary ...

Journal: :journal of research in health sciences 0
h pour-jafari f emami mr mohammad hassani

background: essential hypertension tends to a familial mode. its pattern of inheritance is heterogeneous, but the frequencies of different mode of inheritance vary in different populations. determining of the mode of inheritance in each family is the basic information that is needed for the risk estimation in those family members. determination of pattern of inheritance in families with at leas...

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