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Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology
|
May 10, 2013
Travelling after amniocentesis: answer to a frequent question
K E Karaşahin, M Ozturk, H Çoksuer, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 28, 2018
Central nervous system abnormalities and psychomotor retardation in a girl with a 15.4-MB deletion of 14q12→q21.2 and a 550-KB deletion of 18p11.23: microarray delineation of an unbalanced chromosome rearrangement and a literature review
D Torun, M Arslan, H Akar, et al.
Annales De Genetique
|
May 20, 2000
Hypomelanosis of ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicism
Y Tunca, R S Wilroy, J S Kadandale, et al.
American Journal of Medical Genetics
|
November 14, 2000
Localization of SRY by primed in situ labeling in XX and XY sex reversal
J S Kadandale, S S Wachtel, Y Tunca, et al.
Allergologia Et Immunopathologia
|
August 6, 2008
The role of ace gene polymorphism in the development of angioedema secondary to angiotensin converting enzyme inhibitors and angiotensin II receptor blockers
M Gulec, Z Caliskaner, Y Tunca, et al.
Prenatal Diagnosis
|
October 8, 1997
Application of the 'Apt test' in prenatal diagnosis to evaluate the fetal origin of blood obtained by cordocentesis: results of 30 pregnancies
G Ogur, D Gül, S Ozen, et al.
International Journal of Immunogenetics
|
June 4, 2010
The rate of MEFV gene mutations in hematolymphoid neoplasms
S Celik, A A Erikci, Y Tunca, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology
|
May 10, 2013
Travelling after amniocentesis: answer to a frequent question
K E Karaşahin, M Ozturk, H Çoksuer, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 28, 2018
Central nervous system abnormalities and psychomotor retardation in a girl with a 15.4-MB deletion of 14q12→q21.2 and a 550-KB deletion of 18p11.23: microarray delineation of an unbalanced chromosome rearrangement and a literature review
D Torun, M Arslan, H Akar, et al.
Annales De Genetique
|
May 20, 2000
Hypomelanosis of ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicism
Y Tunca, R S Wilroy, J S Kadandale, et al.
American Journal of Medical Genetics
|
November 14, 2000
Localization of SRY by primed in situ labeling in XX and XY sex reversal
J S Kadandale, S S Wachtel, Y Tunca, et al.
Allergologia Et Immunopathologia
|
August 6, 2008
The role of ace gene polymorphism in the development of angioedema secondary to angiotensin converting enzyme inhibitors and angiotensin II receptor blockers
M Gulec, Z Caliskaner, Y Tunca, et al.
Prenatal Diagnosis
|
October 8, 1997
Application of the 'Apt test' in prenatal diagnosis to evaluate the fetal origin of blood obtained by cordocentesis: results of 30 pregnancies
G Ogur, D Gül, S Ozen, et al.
International Journal of Immunogenetics
|
June 4, 2010
The rate of MEFV gene mutations in hematolymphoid neoplasms
S Celik, A A Erikci, Y Tunca, et al.
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of 2