Molecular diagnosis of duchenne muscular dystrophy in Singapore

Molecular diagnosis of duchenne muscular dystrophy in Singapore

Annals of the Academy of Medicine Singapore

Saved in:

書目詳細資料
Main Authors:	Low, P.S., Lai, P.S., Lee, W.L., Chin, S.M., Tay, J.S.H., Ong, H.T.
其他作者:	PAEDIATRICS
格式:	Article
出版:	2013
主題:	Carrier detection Deletion mutation DNA analysis Linkage analysis Prenatal diagnosis
在線閱讀:	http://scholarbank.nus.edu.sg/handle/10635/48003
標簽:	添加標簽沒有標簽, 成為第一個標記此記錄!

相似書籍

Dimeric gold nanoparticle assembly for detection and discrimination of single nucleotide mutation in Duchenne muscular dystrophy
由: Qin, W.J., et al.
出版: (2011)

Transaminitis in Duchenne's muscular dystrophy
由: Tay, S.K.H., et al.
出版: (2016)

Pathogenesis of Duchenne muscular dystrophy: The calcium hypothesis revisited
由: Tay, J.S.H., et al.
出版: (2013)

Duchenne Muscular Dystrophy - A revisit of the modalities of treatment
由: Low, P.S.
出版: (2013)

Usefulness of dinucleotide polymorphism markers in genetic analysis of Duchenne's muscular dystrophy cases in Singapore.
由: Lai, P.S., et al.
出版: (2013)

Duchenne muscular dystrophy from gene diagnosis to molecular therapy
由: , Masafumi Matsuo
出版: (2003)

DUCHENNE MUSCULAR DYSTROPHY FROM GENE DIAGNOSIS TO MOLECULAR THERAPY
由: , Masafumi Matsuo
出版: (2003)

A two-stage approach identifies a Q344X mutation in the rhodopsin gene of a Chinese Singaporean family with autosomal dominant retinitis pigmentosa
由: Yong, R.Y.Y., et al.
出版: (2016)

Gene repair in duchenne muscular dystrophy
由: CHAN WEI LOONG
出版: (2011)

A manifesting female carrier of Duchenne muscular dystrophy: Importance of genetics for the dystrophinopathies
由: Quak, Zhi Xuan, et al.
出版: (2023)

Genotype and age at diagnosis in Thai boys with Duchenne muscular dystrophy (DMD)
由: Pattareeya Yamputchong, et al.
出版: (2020)

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

Updates on therapies for Duchenne and Becker muscular dystrophy
由: Tay, S.
出版: (2016)

Molecular characterization of β-thalassaemia in Singaporean Chinese: Application to prenatal diagnosis
由: Tan, J.A.M.A., et al.
出版: (2013)

Non-invasive prenatal testing of haemoglobin Bart's Using Fetal DNA from the maternal plasma
由: SHERRY HO SZE YEE
出版: (2010)

Reliability and validity of the Thai version of the Pediatric Quality of Life inventory™ 3.0 Duchenne Muscular Dystrophy module in Thai children with Duchenne Muscular Dystrophy
由: Apirada Thongsing, et al.
出版: (2020)

Sleep disordered breathing in young boys with duchenne muscular dystrophy
由: Hemant Sawnani, et al.
出版: (2018)

Duchenne muscular dystrophy in northeastern Thai children : a retrospective study
由: Narong Auvichayapat, et al.
出版: (2011)

Peptide-morpholino conjugate: A promising therapeutic for duchenne muscular dystrophy
由: Hong M. Moulton, et al.
出版: (2018)

Duchenne muscular dystrophy in northeastern Thai children : a retrospective study
由: Narong Auvichayapat, et al.
出版: (2007)

X-linked markers in the Duchenne muscular dystrophy gene associated with oral clefts
由: Patel, P.J., et al.
出版: (2016)

Personalised genetic intervention for duchenne muscular dystrophy: Antisense oligomers and exon skipping
由: Chalermchai Mitrpant, et al.
出版: (2018)

Perspectives on Palliative Care Among Duchenne Muscular Dystrophy Patients and Their Families in Singapore
由: Tapawan, Sarah Jane Corpuz, et al.
出版: (2023)

Diagnosis of beta-globin gene mutations in single blastomere by reverse dot blot hybridization
由: Jiraporn Pansatha
出版: (2006)

Diagnosis of beta-globin gene mutations in single blastomere by reverse dot blot hybridization
由: Jiraporn Pansatha
出版: (2003)

Long-term Follow-up of Pulmonary Function and Scoliosis in Patients With Duchenne's Muscular Dystrophy and Spinal Muscular Atrophy
由: Chua, Kenon, et al.
出版: (2023)

Clinical practice with steroid therapy for Duchenne muscular dystrophy: An expert survey in Asia and Oceania
由: Fumi Takeuchi, et al.
出版: (2020)

Exome Analysis of Two Limb-Girdle Muscular Dystrophy Families: Mutations Identified and Challenges Encountered
由: McDonald K.K., et al.
出版: (2019)

Non-ambulatory Duchenne muscular dystrophy: observations, interventions, and outcomes of a single case
由: Noer, Sevria Yetty Anggraina, et al.
出版: (2022)

Non-ambulatory Duchenne muscular dystrophy: observations, interventions, and outcomes on a single case
由: Noer, Sevria Yetty Anggraina, et al.
出版: (2022)

DIRECT REPEATS AND DELETIONS IN MITOCHONDRIAL DNA: CASUAL AND EVOLUTIONARY ASPECTS
由: LAKSHMI NARAYANAN LAKSHMANAN
出版: (2014)

PDGFRα signalling promotes fibrogenic responses in collagen-producing cells in Duchenne muscular dystrophy
由: Nicholas Ieronimakis, et al.
出版: (2018)

Muscular dystrophy. Muscular dystrophy in white Pekin Ducks
由: Gopalakrishnakone, P.
出版: (2012)

Application of Computational Intelligence for Faulty Detection and Diagnosis of Induction Motors and electromechanical Systems
由: ZHANG YIFAN
出版: (2013)

Muscular dystrophy in the duck
由: Gopalakrishnakone, P., et al.
出版: (2012)

Linkage disequilibrium between two loci (5' untranslated exon 1 and intron 5-DdeI) of the antithrombin III gene in three ethnic groups in Singapore
由: Liu, Y., et al.
出版: (2013)

Muscular dystrophy model
由: Saranyapin Potikanond, et al.
出版: (2018)

Congestive heart failure with rhabdomyolysis and acute renal failure in a manifesting female carrier of duchenne muscular dystrophy with duplication of dystrophin gene
由: Atchara Tunteeratum, et al.
出版: (2018)

Applications of Multiv Ariate Analysis Techniques for Fault Detection, Diagnosis and Isolation
由: PREM KRISHNAN
出版: (2012)

Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain
由: Allamand, V, et al.
出版: (2020)