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3by Mahaletchumi, Morgan, Nor Rul Hasma, Abdullah, M. H., Sulaiman, Mahfuzah, Mustafa, Rosdiyana, Samad“… of the evolutionary programming. Hence, in this paper, an adaptive mutation operator based multi-objective…”
Published 2015
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4by Nowrin, Shifat A, Basri, Rehana, Alam, Mohammad Khursheed, Yusa, Tatsunori, Nakano, Junzaburo, Jaafar, Saidi, Mokhtar, Khairani Idah, Osuga, Naoto“… of craniofacial structures of DUSP6 gene mutation and non-mutation groups in class III malocclusion of Malaysian…”
Published 2016
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6“… possibility to mutate, that is, to change into a gene of the other kind. We investigate the derived models…”
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7“…. For instance, a yellow buttery may have a black offspring. This kind of variation and mutation, though rare…”
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10by Mahaletchumi, Morgan, Nor Rul Hasma, Abdullah, M. H., Sulaiman, Mahfuzah, Mustafa, Rosdiyana, Samad“…, this research involves development of an adaptive mutation algorithm based multi-objective for Optimal…”
Published 2016
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11by Muhamad Zamil, Nabilah, Mohamed Yussof, Nor Aini, Ardini, Yunita Dewi, Lestari, Widya“… recorded in Malaysia (2.8%). This study aimed to identify any mutation of MSX1 in Malaysian family…”
Published 2018
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13by Nowrin, Shifat A, Basri, Rehana, Alam, Mohammad Khursheed, Jaafar, Saidi, Mokhtar@Makhtar, Khairani Idah“… of mutation and non mutation group in class III malocclusion of Malaysian Malay families and their three…”
Published 2016
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14by Nor Azian Abdul Murad, Saiful Effendi Syafruddin, Muhiddin Ishak, Mohd Ridhwan Abdul Razak, Sri Noraima Othman, Soon, Bee Hong, Azizi Abu Bakar, Farizal Fadzil, Jegan Thanabalan, Toh, Charng Jeng, Isa Mohamed Rose, Roslan Harun, Rahman Jamal“… alterations and mutations have been identified in glioma using various approaches. We performed DNA sequencing…”
Published 2016
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15by Nowrin, Shifat A., Basri, Rehana, Alam, Mohammad Khursheed, Jaafar, Saidi, Mokhtar@Makhtar, Khairani Idah“…Objective: To determine the DUSP6 gene mutation in three generations of Malaysian Malay subjects…”
Published 2019
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16by Mohamed Idrus, Nur Farahiyah, Rosley, Nur Syahira, Irfanita, Nining, Ardini, Yunita Dewi, Arief Ichwan, Solachuddin Jauhari, Lestari, Widya“… of the genes that caused non-syndromic hypodontia. We aimed to investigate the PAX9 mutation of non-syndromic…”
Published 2016
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17by Mohamed Idrus, Nur Farahiyah, Rosley, Nur Syahira, Irfanita, Nining, Ardini, Yunita Dewi, Ichwan, Solachuddin J. A., Lestari, Widya“… of the genes that caused non-syndromic hypodontia. We aimed to investigate the PAX9 mutation of non-syndromic…”
Published 2016
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18by Lestari, Widya“… the PAX9 mutation of non-syndromic hypodontia with clinical variability in Malaysian hypodontia families…”
Published 2016
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20by Zainuddin, Norafiza, Murray, Fiona, Kanduri, Meena, Gunnarsson, Rebeqa, E. Smedby, Karin, Enblad, Gunilla, Jurlander, Jesper, Juliusson, Gunnar, Rosenquist, Richard“…TP53 mutations in the absence of 17p-deletion correlate with rapid disease progression and poor…”
Published 2011
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