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Balkan Journal of Medical Genetics : BJMG
|
October 17, 2022
Determination of Cystic Fibrosis Mutation Frequency in Preterm and Term Neonates with Respiratory Tract Problems
S Tanriverdi, M Polat, H Onay
Acta Endocrinologica (Bucharest, Romania : 2005)
|
October 10, 2022
CONGENITAL ADRENAL HYPERPLASIA WITH COMPOUND HETEROZYGOUS I2 SPLICE AND P453S MUTATIONS
B Almacan, N Ozdemir, H Onay, et al.
Urologia Internationalis
|
July 31, 2009
Multigene methylation analysis of conventional renal cell carcinoma
H Onay, S Pehlivan, M Koyuncuoglu, et al.
Genetic Counseling (Geneva, Switzerland)
|
September 12, 2018
GENETIC COUNSELLING IN FEINGOLD SYNDROME AND A NOVEL MUTATION
T Atik, M S Güvenç, H Onay, et al.
Genetic Counseling (Geneva, Switzerland)
|
September 10, 2015
CLINICAL VARIABILITY IN TWO SISTERS WITH KEUTEL SYNDROME DUE TO A HOMOZYGOUS MUTATION IN MGP GENE
B Tüysüz, B Cinar, S Laçiner, et al.
Balkan Journal of Medical Genetics : BJMG
|
April 30, 2014
Determination of fetal rhesus d status by maternal plasma DNA analysis
A Aykut, H Onay, S Sagol, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 23, 2005
Two extra euchromatic bands in the qh region of chromosome 9
F Ozkinay, D Ercal, C Ozkinay, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 11, 2012
A cardio-facio-cutaneous syndrome case with tight Achilles tendons
F Hazan, A Aykut, M Hizarcioglu, et al.
Genetic Counseling (Geneva, Switzerland)
|
March 26, 2015
A twin sibling with Prader-Willi syndrome caused by uniparental disomy conceived after in vitro fertilization
T Atik, A Aykut, E Karaca, et al.
International Journal of Immunogenetics
|
February 8, 2012
Assessment of Toll-like receptor-4 gene polymorphism on pyelonephritis and renal scar
I Akil, F Ozkinay, H Onay, et al.
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of 3
Search research articles
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Showing results (1-10 of 28) with videos related to
Sort By:
Page
of 3
Balkan Journal of Medical Genetics : BJMG
|
October 17, 2022
Determination of Cystic Fibrosis Mutation Frequency in Preterm and Term Neonates with Respiratory Tract Problems
S Tanriverdi, M Polat, H Onay
Acta Endocrinologica (Bucharest, Romania : 2005)
|
October 10, 2022
CONGENITAL ADRENAL HYPERPLASIA WITH COMPOUND HETEROZYGOUS I2 SPLICE AND P453S MUTATIONS
B Almacan, N Ozdemir, H Onay, et al.
Urologia Internationalis
|
July 31, 2009
Multigene methylation analysis of conventional renal cell carcinoma
H Onay, S Pehlivan, M Koyuncuoglu, et al.
Genetic Counseling (Geneva, Switzerland)
|
September 12, 2018
GENETIC COUNSELLING IN FEINGOLD SYNDROME AND A NOVEL MUTATION
T Atik, M S Güvenç, H Onay, et al.
Genetic Counseling (Geneva, Switzerland)
|
September 10, 2015
CLINICAL VARIABILITY IN TWO SISTERS WITH KEUTEL SYNDROME DUE TO A HOMOZYGOUS MUTATION IN MGP GENE
B Tüysüz, B Cinar, S Laçiner, et al.
Balkan Journal of Medical Genetics : BJMG
|
April 30, 2014
Determination of fetal rhesus d status by maternal plasma DNA analysis
A Aykut, H Onay, S Sagol, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 23, 2005
Two extra euchromatic bands in the qh region of chromosome 9
F Ozkinay, D Ercal, C Ozkinay, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 11, 2012
A cardio-facio-cutaneous syndrome case with tight Achilles tendons
F Hazan, A Aykut, M Hizarcioglu, et al.
Genetic Counseling (Geneva, Switzerland)
|
March 26, 2015
A twin sibling with Prader-Willi syndrome caused by uniparental disomy conceived after in vitro fertilization
T Atik, A Aykut, E Karaca, et al.
International Journal of Immunogenetics
|
February 8, 2012
Assessment of Toll-like receptor-4 gene polymorphism on pyelonephritis and renal scar
I Akil, F Ozkinay, H Onay, et al.
Page
of 3