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Experimental Dermatology
|
April 20, 2000
A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions
V M Aita, W Ahmad, A A Panteleyev, et al.
Biomed Research International
|
March 7, 2022
Prediction and Elucidation of Triglycerides Levels Using a Machine Learning and Linear Fuzzy Modelling Approach
Wan Muhamad Amir W Ahmad, Faraz Ahmed, Nor Farid Mohd Noor, et al.
Clinical and Experimental Dermatology
|
September 25, 2014
A novel deletion mutation in the DSG4 gene underlies autosomal recessive hypotrichosis with variable phenotype in two unrelated consanguineous families
A Ullah, S I Raza, R H Ali, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy
|
January 10, 2020
A quercetin based fluorescent chemical sensor for ultra-sensitive determination and speciation of tungsten species in water
G I Mohammed, W Ahmad, H Alwael, et al.
Clinical Genetics
|
August 23, 2006
A novel locus for alopecia with mental retardation syndrome (APMR2) maps to chromosome 3q26.2-q26.31
A Wali, P John, A Gul, et al.
Cureus
|
August 3, 2022
Modeling the Relationship Between Tooth Color and Skin Color in Equations to Predict Tooth Color
Ryhana Mohammmad Zakir Hiyat Moazam, Zuryati Ab-Ghani, Wan Muhamad Amir W Ahmad, et al.
The Malaysian Journal of Medical Sciences : MJMS
|
March 29, 2019
Cortical Modulation After Two Different Repetitive Transcranial Magnetic Stimulation Protocols in Similar Ischemic Stroke Patients
Muhammad Hafiz Hanafi, Nur Karyatee Kassim, Al Hafiz Ibrahim, et al.
Clinical and Experimental Dermatology
|
May 26, 2018
Novel autosomal recessive LAMA3 and PLEC variants underlie junctional epidermolysis bullosa generalized intermediate and epidermolysis bullosa simplex with muscular dystrophy in two consanguineous families
F Ahmad, K Shah, M Umair, et al.
The British Journal of Dermatology
|
January 4, 2012
FZD6 encoding the Wnt receptor frizzled 6 is mutated in autosomal-recessive nail dysplasia
G Naz, S M Pasternack, C Perrin, et al.
Clinical Genetics
|
November 15, 2017
Homozygous XYLT2 variants as a cause of spondyloocular syndrome
M Umair, G Eckstein, G Rudolph, et al.
Page
of 20
Search research articles
Search
Showing results (131-140 of 193) with videos related to
Sort By:
Page
of 20
Experimental Dermatology
|
April 20, 2000
A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions
V M Aita, W Ahmad, A A Panteleyev, et al.
Biomed Research International
|
March 7, 2022
Prediction and Elucidation of Triglycerides Levels Using a Machine Learning and Linear Fuzzy Modelling Approach
Wan Muhamad Amir W Ahmad, Faraz Ahmed, Nor Farid Mohd Noor, et al.
Clinical and Experimental Dermatology
|
September 25, 2014
A novel deletion mutation in the DSG4 gene underlies autosomal recessive hypotrichosis with variable phenotype in two unrelated consanguineous families
A Ullah, S I Raza, R H Ali, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy
|
January 10, 2020
A quercetin based fluorescent chemical sensor for ultra-sensitive determination and speciation of tungsten species in water
G I Mohammed, W Ahmad, H Alwael, et al.
Clinical Genetics
|
August 23, 2006
A novel locus for alopecia with mental retardation syndrome (APMR2) maps to chromosome 3q26.2-q26.31
A Wali, P John, A Gul, et al.
Cureus
|
August 3, 2022
Modeling the Relationship Between Tooth Color and Skin Color in Equations to Predict Tooth Color
Ryhana Mohammmad Zakir Hiyat Moazam, Zuryati Ab-Ghani, Wan Muhamad Amir W Ahmad, et al.
The Malaysian Journal of Medical Sciences : MJMS
|
March 29, 2019
Cortical Modulation After Two Different Repetitive Transcranial Magnetic Stimulation Protocols in Similar Ischemic Stroke Patients
Muhammad Hafiz Hanafi, Nur Karyatee Kassim, Al Hafiz Ibrahim, et al.
Clinical and Experimental Dermatology
|
May 26, 2018
Novel autosomal recessive LAMA3 and PLEC variants underlie junctional epidermolysis bullosa generalized intermediate and epidermolysis bullosa simplex with muscular dystrophy in two consanguineous families
F Ahmad, K Shah, M Umair, et al.
The British Journal of Dermatology
|
January 4, 2012
FZD6 encoding the Wnt receptor frizzled 6 is mutated in autosomal-recessive nail dysplasia
G Naz, S M Pasternack, C Perrin, et al.
Clinical Genetics
|
November 15, 2017
Homozygous XYLT2 variants as a cause of spondyloocular syndrome
M Umair, G Eckstein, G Rudolph, et al.
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of 20