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Clinical Genetics
|
March 21, 2002
Telomere-specific fluorescence in situ hybridization analysis of couples with five or more recurrent miscarriages
S Yakut, S Berker-Karaüzüm, M Simşek, et al.
Balkan Journal of Medical Genetics : BJMG
|
September 21, 2013
Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)
Z Cetin, I Mendilcioglu, S Yakut, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 20, 2016
A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOMPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES
Z Cetin, O Altiok-Clark, S Yakut, et al.
Experimental Oncology
|
October 26, 2005
Novel cytogenetic findings revealed by conventional cytogenetic and FISH analyses in leukaemia patients
S B Karauzum, T Bilgen, I Karadogan, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
July 31, 2014
Prenatal management, pregnancy and pediatric outcomes in fetuses with septated cystic hygroma
C Y Sanhal, I Mendilcioglu, M Ozekinci, et al.
Balkan Journal of Medical Genetics : BJMG
|
September 21, 2013
Mosaic Intrachromosomal Triplication of (12)(p11.2p13) in a Patient with Pallister-Killian Syndrome
S Yakut, E Mihci, O Altiok Clark, et al.
Balkan Journal of Medical Genetics : BJMG
|
September 21, 2013
Aplasia ras homologous member I gene and development of glial tumors
S Yakut, Mr Tuncer, M Berker, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 2, 2005
M-FISH applications in clinical genetics
Z Cetin, S Berker Karaüzüm, S Yakut, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 18 results.
Clinical Genetics
|
March 21, 2002
Telomere-specific fluorescence in situ hybridization analysis of couples with five or more recurrent miscarriages
S Yakut, S Berker-Karaüzüm, M Simşek, et al.
Balkan Journal of Medical Genetics : BJMG
|
September 21, 2013
Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)
Z Cetin, I Mendilcioglu, S Yakut, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 20, 2016
A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOMPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES
Z Cetin, O Altiok-Clark, S Yakut, et al.
Experimental Oncology
|
October 26, 2005
Novel cytogenetic findings revealed by conventional cytogenetic and FISH analyses in leukaemia patients
S B Karauzum, T Bilgen, I Karadogan, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
July 31, 2014
Prenatal management, pregnancy and pediatric outcomes in fetuses with septated cystic hygroma
C Y Sanhal, I Mendilcioglu, M Ozekinci, et al.
Balkan Journal of Medical Genetics : BJMG
|
September 21, 2013
Mosaic Intrachromosomal Triplication of (12)(p11.2p13) in a Patient with Pallister-Killian Syndrome
S Yakut, E Mihci, O Altiok Clark, et al.
Balkan Journal of Medical Genetics : BJMG
|
September 21, 2013
Aplasia ras homologous member I gene and development of glial tumors
S Yakut, Mr Tuncer, M Berker, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 2, 2005
M-FISH applications in clinical genetics
Z Cetin, S Berker Karaüzüm, S Yakut, et al.
Page
of 2