Zobrazeno 1 - 9
of 9
pro vyhledávání: '"M S, Watihayati"'
Autor:
M, Marini, A A, Salmi, M S, Watihayati, M D, SMardziah, M K, Zahri, B P, Hoh, R, Ankathil, P S, Lai, B A, Zilfalil
Publikováno v:
The Medical journal of Malaysia. 63(1)
Duchenne Muscular Dystrophy (DMD) is an X-linked recessive genetic disorder characterized by rapidly progressive muscle weakness. The disease is caused by deletion, duplication or point mutation of the dystrophin gene, located on the X chromosome (Xp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::73841ff7660fea4f973a8bd74ca7a588
https://pubmed.ncbi.nlm.nih.gov/18935728
https://pubmed.ncbi.nlm.nih.gov/18935728
Autor:
Amin Baig Atif, Teguh Haryo Sasongko, Bin Alwi Zilfalil, Thean-Hock Tang, Z A M H Zabidi-Hussin, Hayati Fatemeh, M S Watihayati, Wan Mohd Zahiruddin, Marzuki Marini, Hisahide Nishio
Publikováno v:
Braindevelopment. 31(1)
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder caused by mutations in the SMN1 gene. The SMN2 gene is highly homologous to SMN1 and has been reported to be correlated with severity of the disease. The clinical presenta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5018e25ff8feac890a81bee81ff4881a
https://pubmed.ncbi.nlm.nih.gov/18842367
https://pubmed.ncbi.nlm.nih.gov/18842367
Autor:
Gunadi, Fatemeh Hayati, M S Watihayati, Manickam Ravichandran, Bin Alwi Zilfalil, Hisahide Nishio, Amin Baig Atif, Teguh Haryo Sasongko, Z A M H Zabidi-Hussin, Marzuki Marini
Publikováno v:
The Indian Journal of Medical Research
Background & objectives: Genetic diagnosis of spinal muscular atrophy (SMA) is complicated by the presence of SMN2 gene as majority of SMA patients show absence or deletion of SMN1 gene. PCR may amplify both the genes non selectively in presence of h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71d2a92863c746a0bbe0f479008d5dee
https://doi.org/10.4103/0971-5916.93421
https://doi.org/10.4103/0971-5916.93421
Publikováno v:
Malaysian Journal of Medical Sciences. Jul2008 Supplement, p37-37. 1p.
Publikováno v:
Malaysian Journal of Medical Sciences. Jul2008 Supplement, p36-36. 1p.
Autor:
H., Fatemeh1, M. S., Watihayati1, M., Marini1, A. B., Atif1, A. A., Che Badariah2, B. A., Zilfalil1
Publikováno v:
Malaysian Journal of Medical Sciences. Jul2008 Supplement, p30-30. 1p.
Publikováno v:
Malaysian Journal of Medical Sciences. Jan2006 Supplement, Vol. 13, p101-101. 1p.
Autor:
M. S., Watihayati1, B. A., Zilfalil1, T. H., Sasongko2, T. H., Tang3, A. M. H., Zabidi-Husin4, H., Nishio2
Publikováno v:
Malaysian Journal of Medical Sciences. Jan2006 Supplement, Vol. 13, p95-95. 1p.
Autor:
Watihayati MS; Human Genome Centre, Universiti Sains Malaysia, Malaysia., Zabidi AM, Tang TH, Nishio H, Zilfalil BA
Publikováno v:
The Kobe journal of medical sciences [Kobe J Med Sci] 2007; Vol. 53 (4), pp. 171-5.