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Genetic Counseling (Geneva, Switzerland)
|
November 3, 2004
Laryngomalacia, choanal atresia and renal anomaly in a newborn with Freeman-Sheldon syndrome phenotype
A Tastekin, M Ikbal, R Ors
Genetic Counseling (Geneva, Switzerland)
|
August 4, 2004
Micropenis in a newborn with acrocallosal syndrome
M Ikbal, A Tastekin, R Ors
Toxicology and Industrial Health
|
June 2, 2009
Protective role of vitamins A, C, and E against the genotoxic damage induced by aflatoxin B1 in cultured human lymphocytes
L Alpsoy, G Agar, M Ikbal
American Journal of Medical Genetics. Part A
|
December 24, 2004
Response to Devriendt et al. "Pulmonary atresia/ventricular septal defect associated with facial port-wine stain and retinal vascular abnormality"
H Tan, M Ikbal, N Ceviz
Heliyon
|
July 26, 2021
Automotive suspension component behaviors driven on flat and rough road surfaces
T E Putra, Husaini, M Ikbal
Annals of the Rheumatic Diseases
|
July 16, 2003
Association of sister chromatid exchange frequencies in patients with ankylosing spondylitis with and without HLA-B27
M Ikbal, N Ezirmik, T Tos, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 4, 2004
Pectus excavatum and situs inversus totalis: a new combination or a coincidence?
A Eroğlu, I C Kürkçüoğlu, N Karaoğlanoğlu, et al.
Tissue Antigens
|
August 12, 2004
HLA class I and class II genotyping in patients with Behcet's disease: a regional study of eastern part of Turkey
I Pirim, M Atasoy, M Ikbal, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 1, 2006
Linear atrophoderma of Moulin together with leuconychia: a case report
M Atasoy, C Aliagaoglu, O Sahin, et al.
Mutation Research
|
December 11, 1997
Sister chromatid exchange analysis in patients exposed to low dose of iodine-131 for thyroid scintigraphy
S Sönmez, M Ikbal, M Yíldírím, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 31) with videos related to
Sort By:
Page
of 4
Genetic Counseling (Geneva, Switzerland)
|
November 3, 2004
Laryngomalacia, choanal atresia and renal anomaly in a newborn with Freeman-Sheldon syndrome phenotype
A Tastekin, M Ikbal, R Ors
Genetic Counseling (Geneva, Switzerland)
|
August 4, 2004
Micropenis in a newborn with acrocallosal syndrome
M Ikbal, A Tastekin, R Ors
Toxicology and Industrial Health
|
June 2, 2009
Protective role of vitamins A, C, and E against the genotoxic damage induced by aflatoxin B1 in cultured human lymphocytes
L Alpsoy, G Agar, M Ikbal
American Journal of Medical Genetics. Part A
|
December 24, 2004
Response to Devriendt et al. "Pulmonary atresia/ventricular septal defect associated with facial port-wine stain and retinal vascular abnormality"
H Tan, M Ikbal, N Ceviz
Heliyon
|
July 26, 2021
Automotive suspension component behaviors driven on flat and rough road surfaces
T E Putra, Husaini, M Ikbal
Annals of the Rheumatic Diseases
|
July 16, 2003
Association of sister chromatid exchange frequencies in patients with ankylosing spondylitis with and without HLA-B27
M Ikbal, N Ezirmik, T Tos, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 4, 2004
Pectus excavatum and situs inversus totalis: a new combination or a coincidence?
A Eroğlu, I C Kürkçüoğlu, N Karaoğlanoğlu, et al.
Tissue Antigens
|
August 12, 2004
HLA class I and class II genotyping in patients with Behcet's disease: a regional study of eastern part of Turkey
I Pirim, M Atasoy, M Ikbal, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 1, 2006
Linear atrophoderma of Moulin together with leuconychia: a case report
M Atasoy, C Aliagaoglu, O Sahin, et al.
Mutation Research
|
December 11, 1997
Sister chromatid exchange analysis in patients exposed to low dose of iodine-131 for thyroid scintigraphy
S Sönmez, M Ikbal, M Yíldírím, et al.
Page
of 4