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Simple Search
Hits 1 – 19 of 19
1
Translation and validation of the Chinese version of the MD Anderson symptom inventory for measuring perioperative symptom burden in patients with gynecologic cancer ...
Zhang, Ting
;
Zheng, Ying-ying
;
Yang, Zhi-rong
. - : figshare, 2021
BASE
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2
Translation and validation of the Chinese version of the MD Anderson symptom inventory for measuring perioperative symptom burden in patients with gynecologic cancer ...
Zhang, Ting
;
Zheng, Ying-ying
;
Yang, Zhi-rong
. - : figshare, 2021
BASE
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3
General Facial Representation Learning in a Visual-Linguistic Manner ...
Zheng, Yinglin
;
Yang, Hao
;
Zhang, Ting
. - : arXiv, 2021
BASE
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4
Receptive and Expressive Vocabulary Skills and Their Correlates in Mandarin-Speaking Infants with Unrepaired Cleft Lip and/or Palate
Ma, Si-Wei
;
Lu, Li
;
Zhang, Ting-Ting
...
In: Int J Environ Res Public Health (2020)
BASE
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5
Correlation between clinical parameters of crown and gingival morphology of anterior teeth and periodontal biotypes
Yin, Xiao-jie
;
Wei, Bang-yan
;
Ke, Xiu-ping
. - : BioMed Central, 2020
BASE
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6
Dynamic methylome of internal mRNA N(7)-methylguanosine and its regulatory role in translation
Malbec, Lionel
;
Zhang, Ting
;
Chen, Yu-Sheng
...
In: Cell Res (2019)
BASE
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7
A DAF-3 co-Smad molecule functions in Haemonchus contortus development
Di, Wenda
;
Liu, Lu
;
Zhang, Ting
. - : BioMed Central, 2019
BASE
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8
Differences in Cardiorespiratory Fitness between Chinese and Japanese Children and Adolescents
Yang, Xiaofang
;
Yin, Xiaojian
;
Ji, Liu
. - : MDPI, 2019
BASE
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9
Online comics for the teaching and learning of Chinese language in the Australian context
Zhang, Ting
. - 2019
BASE
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10
Triphenyl phosphite as the phosphorus source for the scalable and cost-effective production of transition metal phosphides
Liu, Junfeng
;
Meyns, Michaela
;
Zhang, Ting
. - : American Chemical Society, 2018
BASE
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11
Beyond the traditional simulation design for evaluating type 1 error control: From the “theoretical” null to “empirical” null
Zhang, Ting
;
Sun, Lei
. - : John Wiley and Sons Inc., 2018
BASE
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12
Vocationally oriented English training in Chinese technical and vocational colleges : take the major "Industrial analysis and test" as an example
Zhang, Ting
[Verfasser]. - 2017
DNB Subject Category Language
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13
Segmental and tonal errors in L2 Mandarin speech produced by Australian English learners
Zhang, Ting
;
Tsurutani, Chiharu
;
Gu, Wentao
. - : Australasian Speech Science and Technology Association (ASSTA), 2014
BASE
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14
THE ROLE OF READING COMPREHENSION IN LARGE-SCALE SUBJECT-MATTER ASSESSMENTS
Zhang, Ting
. - 2013
BASE
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15
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.
Ching, Michael SL
;
Shen, Yiping
;
Tan, Wen-Hann
;
Jeste, Shafali S
;
Morrow, Eric M
;
Chen, Xiaoli
;
Mukaddes, Nahit M
;
Yoo, Seung-Yun
;
Hanson, Ellen
;
Hundley, Rachel
;
Austin, Christina
;
Becker, Ronald E
;
Berry, Gerard T
;
Driscoll, Katherine
;
Engle, Elizabeth C
;
Friedman, Sandra
;
Gusella, James F
;
Hisama, Fuki M
;
Irons, Mira B
;
Lafiosca, Tina
;
LeClair, Elaine
;
Miller, David T
;
Neessen, Michael
;
Picker, Jonathan D
;
Rappaport, Leonard
;
Rooney, Cynthia M
;
Sarco, Dean P
;
Stoler, Joan M
;
Walsh, Christopher A
;
Wolff, Robert R
;
Zhang, Ting
;
Nasir, Ramzi H
;
Wu, Bai-Lin
;
Children's Hospital Boston Genotype Phenotype Study Group
In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, vol 153B, iss 4 (2010)
Abstract:
Research has implicated mutations in the gene for neurexin-1 (NRXN1) in a variety of conditions including autism, schizophrenia, and nicotine dependence. To our knowledge, there have been no published reports describing the breadth of the phenotype associated with mutations in NRXN1. We present a medical record review of subjects with deletions involving exonic sequences of NRXN1. We ascertained cases from 3,540 individuals referred clinically for comparative genomic hybridization testing from March 2007 to January 2009. Twelve subjects were identified with exonic deletions. The phenotype of individuals with NRXN1 deletion is variable and includes autism spectrum disorders, mental retardation, language delays, and hypotonia. There was a statistically significant increase in NRXN1 deletion in our clinical sample compared to control populations described in the literature (P = 8.9 x 10(-7)). Three additional subjects with NRXN1 deletions and autism were identified through the Homozygosity Mapping Collaborative for Autism, and this deletion segregated with the phenotype. Our study indicates that deletions of NRXN1 predispose to a wide spectrum of developmental disorders.
Keyword:
array CGH
;
Autistic Disorder
;
Child
;
Child Development Disorders
;
Children's Hospital Boston Genotype Phenotype Study Group
;
Clinical Sciences
;
CNV
;
Comparative Genomic Hybridization
;
Developmental Disabilities
;
developmental disorders
;
Female
;
Genetics
;
Humans
;
Intellectual Disability
;
Language Development Disorders
;
Male
;
Mutation
;
Neurosciences
;
NRXN1
;
NRXN1 exonic deletions
;
Pervasive
;
Phenotype
;
Schizophrenia
;
Sequence Deletion
URL:
https://escholarship.org/uc/item/6zj2639n
BASE
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16
Frequency overlap between electric and acoustic stimulation and speech-perception benefit in patients with combined electric and acoustic stimulation
Zhang, Ting
;
Spahr, Anthony J.
;
Dorman, Michael F.
. - 2010
BASE
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17
Situational Context and Marked Code-Switching
DONG, Mao-di
;
ZHANG, Ting-guo
In: Cross-Cultural Communication; Vol 5, No 1 (2009): Cross-Cultural Communication; 62-67 ; 1923-6700 ; 1712-8358 (2010)
BASE
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18
The benefits of acoustic input to combined electric and contralateral acoustic hearing
Zhang, Ting
. - 2008
BASE
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19
Effects of cueing in auditory temporal masking
Zhang, Ting
;
Formby, Craig
In:
Journal of speech, language, and hearing research. - Rockville, Md. : American Speech-Language-Hearing Association
50 (2007) 3, 564-575
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