Genetic studies of Prader-Willi patients from Taiwan identify two patients with atypical deletions and provide evidences for conservation of genomic architecture in proximal chromosome 15q

Genetic studies of Prader-Willi patients from Taiwan identify two patients with atypical deletions and provide evidences for conservation of genomic architecture in proximal chromosome 15q

Prader-Willi syndrome (PWS) is a neurogenetic disorder associated with recurrent genomic recombination involving low copy repeats (LCRs) located in the human chromosome 15q11-q13. Previous studies of PWS patients from Asia suggested that there is a higher incidence of deletion and lower incidence of...

Saved in:

書目詳細資料
Main Authors:	Lin, Shuan Pei., Ho, Shi Yun., Chen, Yen Jiun., Huang, Chi Yu., Chiu, Hui Ching., Chuang, Chih Kuang., Hou, Aihua., Chen, Jennifer Chi Fung., Lin, Hsiang Yu., Chen, Ken-Shiung.
其他作者:	School of Biological Sciences
格式:	Article
語言:	English
出版:	2011
主題:	DRNTU::Science::Biological sciences::Genetics
在線閱讀:	https://hdl.handle.net/10356/94104 http://hdl.handle.net/10220/7172
標簽:	添加標簽沒有標簽, 成為第一個標記此記錄!

相似書籍

Molecular markers for diagnosis of prader-willi syndrome in thai patients by fish
由: Sirilak Wiriyaukaradecha, et al.
出版: (2018)

Detection and discrimination between deletional and non-deletional prader-willi and angelman syndromes by methylation-specific pcr and quantitative melting curve analysis
由: Wang, W., et al.
出版: (2011)

Growth charts for Thai children with Prader-Willi syndrome aged 0-18 years
由: Nantiya Mongkollarp, et al.
出版: (2020)

Cardiac rhabdomyoma as a possible new prenatal sonographic feature of Prader–Willi syndrome
由: Kuntharee Traisrisilp, et al.
出版: (2022)

Cardiac rhabdomyoma as a possible new prenatal sonographic feature of Prader–Willi syndrome
由: Traisrisilp K.
出版: (2023)

Highest accuracy of combined consensus clinical criteria and SNRPN gene molecular markers in diagnosis of Prader-Willi syndrome in Thai patients
由: Moltira Promkan, et al.
出版: (2018)

A 47, XXY patient and Xq21.31 duplication with features of Prader-Willi syndrome: Results of array-based comparative genomic hybridization
由: Pornpoj Pramyothin, et al.
出版: (2018)

The effects of glucagon-like peptide (GLP)-1 receptor agonists on weight and glycaemic control in Prader-Willi syndrome: A systematic review
由: Ng, Nicholas Beng Hui, et al.
出版: (2022)

Chromosome 22q11 deletions in patients with conotruncal heart defects
由: A. Khositseth, et al.
出版: (2018)

Chromosome 10 and 17 deletions and p53 gene mutations in Thai patients with astrocytomas
由: Supawadee Put-Ti-Noi, et al.
出版: (2018)

Atypical SARS in Geriatric Patient
由: Tee, A.K.H, et al.
出版: (2020)

Atypical chikungunya virus infections in immunocompromised patients
由: Kee, A.C.L., et al.
出版: (2011)

Willy đi đâu rồi?
由: Allan, Nicholas
出版: (2020)

IS6110-mediated deletions of wild-type chromosomes of Mycobacterium tuberculosis
由: Z. Fang, et al.
出版: (2018)

Chromosomal deletion at 22q11.2 and Parkinson's disease
由: Tan E.-K.
出版: (2018)

Generation of female fibroblast cell lines in which Xist is conditionally and allele-specifically deleted from the inactive X chromosome.
由: Chen, Beibei.
出版: (2012)

Atypical femoral fractures: Epidemiology, etiology, and patient management
由: Eve Donnelly, et al.
出版: (2018)

A simple strategy for heritable chromosomal deletions in zebrafish via the combinatorial action of targeting nucleases
由: Lim, S., et al.
出版: (2014)

Willie’s Point Of View And Reaction Due To His Disappointment To The Government, Capitalism, And Labourer’s Life In Bill Bryden’s Willie Rough
由: Ajeng Kusumawardani
出版: (2005)

Circle of Willis of the brain: anatomical variations and their importance
由: Pasuk Mahakkanukrauh, et al.
出版: (2018)

Circle of Willis of the brain: anatomical variations and their importance
由: Mahakkanukrauh P., et al.
出版: (2017)

ELEMENTS OF SARCASM ON WILLY WONKA INTERNET MEMES
由: MUHAMMAD ADITYA PURNOMO, 121311233038
出版: (2017)

Prevalence of atypical femoral fractures in Thai patients at a single institution
由: Sittichai Luangkittikong, et al.
出版: (2018)

Characterization of atypical lymphocytes and immunophenotypes of lymphocytes in patients with dengue virus infection
由: Wipawee Jampangern, et al.
出版: (2018)

Chromosome 22q11 deletion syndrome : The first three cases reported in Thailand
由: Nichara Ruangdaraganon, et al.
出版: (2018)

Y chromosome gr/gr deletions are a risk factor for low semen quality
由: Visser, L., et al.
出版: (2014)

Willieng Willieng: The study on Willie Revillame's cult following
由: Escay, Mark Joseph D., et al.
出版: (2012)

Multisuture craniosynostosis: a case report of unusual presentation of chromosome 14q32 deletion
由: Chaisrisawadisuk S.
出版: (2023)

AZFc deletions and spermatogenic failure: A population-based survey of 20,000 y chromosomes
由: Rozen, S.G., et al.
出版: (2014)

Chromosome alterations in colorectal cancer in Thai patients
由: S. Poeaim, et al.
出版: (2018)

Megawatts are not megawatt-hours and other responses to Willis et al.
由: Sovacool, B.K.
出版: (2011)

Hospitalization and cost after switching from atypical to typical antipsychotics in schizophrenia patients in Thailand
由: Tuanthon Boonlue, et al.
出版: (2018)

Atypical complication in an adult patient with dengue and autoimmune hemolytic anemia: A case report
由: Supat Chamnanchanunt, et al.
出版: (2022)

Detection of chromosomal breakpoints in patients with developmental delay and speech disorders
由: Utami K.H., et al.
出版: (2018)

The role of the circle of Willis in internal carotid artery stenosis and anatomical variations: a computational study based on a patient-specific three-dimensional model
由: Zhu, Guangyu, et al.
出版: (2015)

Eric Bogle’s No Man’s Land and the grave of Willie McBride at the Somme
由: Walsh, Michael J. K.
出版: (2021)

Willie Revillame: Arketipong bayani at pag-asa ng masang Pilipino
由: Miranda, Mark Anthony C.
出版: (2013)

Sequence reconstruction for deletions
由: Soh, Anna Li Lin
出版: (2023)

Screening of dystrophin gene deletions in Malaysian patients with Duchenne Muscular Dystrophy
由: Marini, M., et al.
出版: (2011)

Finding exclusively deleted or amplified genomic areas in lung adenocarcinomas using a novel chromosomal pattern analysis
由: Brot, P., et al.
出版: (2014)