Search research articles
Contact Us
Filters
Showing results (1-10 of 18) with videos related to
Page
of 2
Sort By:
Australasian Radiology
|
September 22, 2005
Role of magnetic resonance imaging in the early diagnosis of Takayasu arteritis
A M Halefoglu, S Yakut
Genetic Counseling (Geneva, Switzerland)
|
November 5, 2014
Prenatal diagnosis of isochromosome 21p and isochromosome 21q in a fetus with Down syndrome
S Yakut, C Sanhal, E Manguoglu, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 21, 2014
Prenatal diagnosis of isolated ventriculomegaly as a second trimester manifestation of de novo terminal 6q25 deletion
Z Cetin, C Sanhal, B Nur Guzel, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 28, 2018
Ultrasonographic and Cytogenetic Issues in Prenatal Diagnosis of Pallister Killian Syndrome
Z Cetin, C Sanhal, S B Karauzum, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 28, 2011
Interstitial deletion of 13q22-q32: a case with choanal atresia and mega-cisterna magna and review of the literature
Z Cetin, E Mihci, S Yakut, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 19, 2010
Prenatal diagnosis of a de novo supernumerary marker chromosome originating from chromosome 16
S Yakut, Z Cetin, M Simşek, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 28, 2011
De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome
S Yakut, Z Cetin, S Berker-Karauzum, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 28, 2011
Del (18p) syndrome with increased nuchal translucency revealed in prenatal diagnosis
S Yakut, M Simsek, H E Pestereli, et al.
Genetic Counseling (Geneva, Switzerland)
|
September 10, 2015
PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13)
S Yakut, Z Cetin, C Sanhal, et al.
Genetic Counseling (Geneva, Switzerland)
|
December 3, 2015
PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGH
S Yakut, Z Cetin, C Sanhal, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
Australasian Radiology
|
September 22, 2005
Role of magnetic resonance imaging in the early diagnosis of Takayasu arteritis
A M Halefoglu, S Yakut
Genetic Counseling (Geneva, Switzerland)
|
November 5, 2014
Prenatal diagnosis of isochromosome 21p and isochromosome 21q in a fetus with Down syndrome
S Yakut, C Sanhal, E Manguoglu, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 21, 2014
Prenatal diagnosis of isolated ventriculomegaly as a second trimester manifestation of de novo terminal 6q25 deletion
Z Cetin, C Sanhal, B Nur Guzel, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 28, 2018
Ultrasonographic and Cytogenetic Issues in Prenatal Diagnosis of Pallister Killian Syndrome
Z Cetin, C Sanhal, S B Karauzum, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 28, 2011
Interstitial deletion of 13q22-q32: a case with choanal atresia and mega-cisterna magna and review of the literature
Z Cetin, E Mihci, S Yakut, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 19, 2010
Prenatal diagnosis of a de novo supernumerary marker chromosome originating from chromosome 16
S Yakut, Z Cetin, M Simşek, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 28, 2011
De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome
S Yakut, Z Cetin, S Berker-Karauzum, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 28, 2011
Del (18p) syndrome with increased nuchal translucency revealed in prenatal diagnosis
S Yakut, M Simsek, H E Pestereli, et al.
Genetic Counseling (Geneva, Switzerland)
|
September 10, 2015
PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13)
S Yakut, Z Cetin, C Sanhal, et al.
Genetic Counseling (Geneva, Switzerland)
|
December 3, 2015
PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGH
S Yakut, Z Cetin, C Sanhal, et al.
Page
of 2