نتایج جستجو برای: bukowitz and williams

تعداد نتایج: 16828942  

Journal: :Neuropsychologia 2006
Janette Atkinson Oliver Braddick Fredric E Rose Yvonne M Searcy John Wattam-Bell Ursula Bellugi

Previous studies of children with Williams syndrome (WS) have found a specific deficit in dorsal cortical stream function, indicated by poor performance in coherence thresholds for motion compared to form. Here we investigated whether this is a transient developmental feature or a persisting aspect of cerebral organization in WS. Motion and form coherence thresholds were tested in a group of 45...

Journal: :journal of research in health sciences 0
amal saki malehi ebrahim hajizadeh kambiz ahmadi nahid kholdi

background: this study aimes to evaluate the failure to thrive (ftt) recurrent event over time. methods: this longitudinal study was conducted during february 2007 to july 2009. the primary outcome was growth failure. the analysis was done using 1283 children who had experienced ftt several times, based on recurrent events analysis. results: fifty-nine percent of the children had experienced th...

2003
Michael Thomas Eleanor Semel Annette Karmiloff-Smith Dagmara Annaz Sue Rosner

2016
J. Barter

Slit.?With reference to a note on page 287 of the September Gazette, to the effect that Miss Anna Williams won His Excellency's silver medal. &c., the facts are these. Anna Williams, a Native Christian pupil, won a medal offered for competition by a lady in the Central Proviuces. His Excellency the Viceroy has not given a prize for competition by the Nagpur class, which is confined strictly to ...

Journal: :نامه انجمن حشره شناسی ایران 0
معصومه مقدم نادر آزادبخت

scale insect specimens collected on hordeum sp. (poaceae), dated 24. v. 2003 in khorram abad, lorestan province were identified as exaeretopus tritici williams. this species, which the genus and species is newly recorded from iran, is related to e. harpazi ben-dov, differing mainly in the number of the stigmatic setae and extension of paraopercular pores.

Journal: : 2021

Hội chứng Williams (Williams Syndrome -WS) là bệnh di truyền hiếm gặp, do mất đoạn nhỏ trên cánh dài nhiễm sắc thể (NST) số 7 (7q11.23). Tỉ lệ mắc 1/7.500 - 10.000 trẻ đẻ sống. WS đặc trưng bởi khuôn mặt bất thường, dị tật tim và tính cách quá hòa đồng.
 Mục tiêu: Phát hiện 7q11.23 bằng kỹ thuật lai huỳnh quang tại chỗ (Flurorescen in situ Hybridizaton FISH).
 Phương pháp: Mười bảy nh...

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