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Results of search for 'au:"Zilfalil, B-A"', page 1 of 2
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Authors
Ankathil, R
Azman, B Z
Bhuiyan, Z A
Halim, A S
Hoh, B P
Ismail, R
Kannan, T P
Liza-Sharmini, A T
Marini, M
Narazah, M Y
Nishio, H
Nizam, M Z
Nor Atifah, M A
Pal, S
Salahshourifar, I
Siti Mariam, I
Suhaida, M A
Teh, L K
Watihayati, M S
Zilfalil, B A
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Topics
Abnormalities, Multiple
Adolescent
Adult
Asian People
Child
Child, Preschool
Female
Genotype
Humans
Infant
Infant, Newborn
Karyotyping
Malaysia
Male
Mutation
Polymerase Chain Reaction
Polymorphism, Genetic
diagnosis
genetics
methods
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English
Your search returned 22 results.
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Results
1.
Prevalence and molecular study of G6PD deficiency in Malaysian Orang Asli.
[electronic resource]
by
Amini, F
Ismail, E
Zilfalil, B-A
Producer:
20120306
In:
Internal medicine journal
vol. 41
Online resources:
Available from publisher's website
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No items available.
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2.
Clinical and genetic analysis of long QT syndrome in two Malay children.
[electronic resource]
by
Wong, A R
Zilfalil, B A
Bhuiyan, Z A
Producer:
20200617
In:
The Medical journal of Malaysia
vol. 74
Availability:
No items available.
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3.
Ocular findings in Malaysian children with Down syndrome.
[electronic resource]
by
Liza-Sharmini, A T
Azlan, Z N
Zilfalil, B A
Producer:
20060221
In:
Singapore medical journal
vol. 47
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No items available.
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4.
Clinical manifestations in trisomy 9.
[electronic resource]
by
Kannan, T P
Hemlatha, S
Ankathil, R
Zilfalil, B A
Producer:
20100302
In:
Indian journal of pediatrics
vol. 76
Online resources:
Available from publisher's website
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5.
A Malay boy with the Cornelia de Lange syndrome: clinical and molecular findings.
[electronic resource]
by
Bhuiyan, Z A
Zilfalil, B A
Hennekam, R C M
Producer:
20061012
In:
Singapore medical journal
vol. 47
Availability:
No items available.
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6.
Two cases of isochromosome 18q syndrome.
[electronic resource]
by
Pal, S
Siti, M I
Ankathil, R
Zilfalil, B A
Producer:
20070521
In:
Singapore medical journal
vol. 48
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7.
Two cases of deletion 5p syndrome: one with paternal involvement and another with atypical presentation.
[electronic resource]
by
Azman, B Z
Akhir, S M
Zilfalil, B A
Ankathil, R
Producer:
20080623
In:
Singapore medical journal
vol. 49
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8.
Contribution of 6p24 to non-syndromic cleft lip and palate in a Malay population: association of variants in OFC1.
[electronic resource]
by
Salahshourifar, I
Halim, A S
Sulaiman, W A W
Zilfalil, B A
Producer:
20110322
In:
Journal of dental research
vol. 90
Online resources:
Available from publisher's website
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9.
Genetic polymorphism of CYP2D6 in patients with cardiovascular disease -- a cohort study.
[electronic resource]
by
Teh, L K
Zilfalil, B A
Marina, I
Rosemi, B S
Ismail, R
Producer:
20050412
In:
Journal of clinical pharmacy and therapeutics
vol. 29
Online resources:
Available from publisher's website
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10.
Detection of F508del mutation in cystic fibrosis transmembrane conductance regulator gene mutation among Malays.
[electronic resource]
by
Zilfalil, B A
Sarina, S
Liza-Sharmini, A T
Oldfield, N J
Stenhouse, S A
Producer:
20060505
In:
Singapore medical journal
vol. 47
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11.
Screening for gap junction protein beta-2 gene mutations in Malays with autosomal recessive, non-syndromic hearing loss, using denaturing high performance liquid chromatography.
[electronic resource]
by
Aishah, Z Siti
Khairi, M D Mohd
Normastura, A R
Zafarina, Z
Zilfalil, B A
Producer:
20090219
In:
The Journal of laryngology and otology
vol. 122
Online resources:
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12.
Chromosomal abnormalities and reproductive outcome in Malaysian couples with miscarriages.
[electronic resource]
by
Pal, S
Ma, S O
Norhasimah, M
Suhaida, M A
Siti Mariam, I
Ankathil, R
Zilfalil, B A
Producer:
20100218
In:
Singapore medical journal
vol. 50
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No items available.
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13.
De novo interstitial deletion of 1q32.2-q32.3 including the entire IRF6 gene in a patient with oral cleft and other dysmorphic features.
[electronic resource]
by
Salahshourifar, I
Halim, A S
Sulaiman, W A W
Ariffin, R
Naili Muhamad Nor, N
Zilfalil, B A
Producer:
20110708
In:
Cytogenetic and genome research
vol. 134
Online resources:
Available from publisher's website
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14.
An improved rapid genotyping method for the study of beta-2 adrenergic receptor gene polymorphisms using single tube allele specific multiplex PCR.
[electronic resource]
by
Zilfalil, B A
Hoh, B P
Nizam, M Z
Liza-Sharmini, A T
Teh, L K
Ismail, R
Producer:
20070124
In:
Journal of clinical pharmacy and therapeutics
vol. 31
Online resources:
Available from publisher's website
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15.
Turner syndrome diagnosed in northeastern Malaysia.
[electronic resource]
by
Kannan, T P
Azman, B Z
Ahmad Tarmizi, A B
Suhaida, M A
Siti Mariam, I
Ravindran, A
Zilfalil, B A
Producer:
20080703
In:
Singapore medical journal
vol. 49
Availability:
No items available.
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16.
Analysis of the survival motor neuron and neuronal apoptosis inhibitory protein genes in Malay patients with Spinal Muscular Atrophy.
[electronic resource]
by
Zilfalil, B A
Zabidi-Hussin, A M H
Watihayati, M S
Rozainah, M Y
Naing, L
Sutomo, R
Nishio, H
Narazah, M Y
Matsuo, M
Producer:
20050512
In:
The Medical journal of Malaysia
vol. 59
Availability:
No items available.
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17.
A simple and rapid genotyping method for beta-2 receptor (beta2 AR) gene using allele specific multiplex PCR.
[electronic resource]
by
Romaino, S M N
Teh, L K
Zilfalil, B A
Thong, C P
Ismail, A A
Amir, J
Salleh, M Z
Noor, A R
Ismail, R
Producer:
20040511
In:
Journal of clinical pharmacy and therapeutics
vol. 29
Online resources:
Available from publisher's website
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18.
Screening of dystrophin gene deletions in Malaysian patients with Duchenne muscular dystrophy.
[electronic resource]
by
Marini, M
Salmi, A A
Watihayati, M S
SMardziah, M D
Zahri, M K
Hoh, B P
Ankathil, R
Lai, P S
Zilfalil, B A
Producer:
20081126
In:
The Medical journal of Malaysia
vol. 63
Availability:
No items available.
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19.
Allele-specific PCR for a cost-effective & time-efficient diagnostic screening of spinal muscular atrophy.
[electronic resource]
by
Marini, M
Sasongko, T H
Watihayati, M S
Atif, A B
Hayati, F
Zabidi-Hussin, Z A M H
Ravichandran, M
Nishio, H
Zilfalil, B A
Producer:
20120612
In:
The Indian journal of medical research
vol. 135
Online resources:
Available from publisher's website
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20.
Cytogenetic and clinical profile of Down syndrome in Northeast Malaysia.
[electronic resource]
by
Azman, B Z
Ankathil, R
Siti Mariam, I
Suhaida, M A
Norhashimah, M
Tarmizi, A B
Nor Atifah, M A
Kannan, T P
Zilfalil, B A
Producer:
20070625
In:
Singapore medical journal
vol. 48
Availability:
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