نتایج جستجو برای: 22 model

تعداد نتایج: 2288996  

Journal: :Clinical dysmorphology 2004
Johannes H Merks Nicolaas Ceelie Huib N Caron Raoul C Hennekam

We report a family with co-occurring disorders including neuroblastoma in the first child conceived by in-vitro fertilization with history of sodium valproate use by the mother during pregnancy and mosaic trisomy 22 in the third child. We discuss the possibility of an association between the disorders but conclude that no firm aetiological connection can be established between the different dis...

پایان نامه :دانشگاه آزاد اسلامی - دانشگاه آزاد اسلامی واحد گرمسار - پژوهشکده علوم انسانی و اجتماعی 1391

abstract the present study was conducted to investigate the effect of using model essays on the development of writing proficiency of iranian pre-intermediate efl learners. to fulfill the purpose of the study, 55 pre- intermediate learners of parsa language institute were chosen by means of administering proficiency test. based on the results of the pretest, two matched groups, one as the expe...

2008
Kimberlie Dean

Three papers in the Journal this month consider issues related to measuring, understanding and treating mental ill health in childhood. Baron-Cohen et al (pp. 500–509) undertook a study to establish the prevalence of autism-spectrum conditions in Cambridgeshire using two case ascertainment methods. First, a survey of individuals on the Special Educational Needs register and second, a screening ...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

2016
M.Ibáñez E.Muñoz

Department of Building and Industrial Production Engineering, University CEU Cardenal Herrera Avda.Seminario s/n, 46113, Moncada, Valencia, Spain Email: [email protected], [email protected], [email protected], [email protected] (*corresponding author), web page: http://www.uchceu.es Departamento de Ingeniería Mecánica y de Materiales, Universidad Politécnica de Vale...

Journal: :Journal of medical genetics 1995
V P Prasher E Roberts A Norman A C Butler V H Krishnan D J McMullan

A case of a 27 year old male with a duplication of part of the long arm of chromosome 22 (22q11.2-q13.1) together with a pericentric inversion of the same chromosome is reported. Particular phenotypic features of note include absence of speech, persistent self-injury, lack of daily living skills, colobomata, and very poor vision. Similarities between this case and other case reports of duplicat...

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