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Z Cetin

Showing results (1-10 of 24) with videos related to

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Genetic Counseling (Geneva, Switzerland)|November 5, 2014
Prenatal diagnosis of isochromosome 21p and isochromosome 21q in a fetus with Down syndromeS Yakut, C Sanhal, E Manguoglu, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13)Z Cetin, E Mihci, I Keser, et al.
Andrologia|January 30, 2014
Ring chromosome 21 and monosomy 21 mosaicism in a patient with azoospermiaZ Cetin, O Altiok-Clark, M Sevuk, et al.
Journal of Investigational Allergology & Clinical Immunology|February 12, 2015
Selective IgM deficiency in a boy with ring chromosome 18F Celmeli, D Turkkahraman, Z Cetin, et al.
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
A PATIENT WITH AZOOSPERMIA AND 45,X/46,X,r(Y) (p11.2q11.2) MOSAICISM WITHOUT AZF DELETIONSO Altiok Clark, I Türker Köksal, S Berker Karaüzüm, et al.
Genetic Counseling (Geneva, Switzerland)|February 21, 2014
Prenatal diagnosis of isolated ventriculomegaly as a second trimester manifestation of de novo terminal 6q25 deletionZ 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 SyndromeZ Cetin, C Sanhal, S B Karauzum, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocationZ Cetin, E Mihci, I Keser, 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 literatureZ Cetin, E Mihci, S Yakut, 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.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Genetic Counseling (Geneva, Switzerland)|November 5, 2014
Prenatal diagnosis of isochromosome 21p and isochromosome 21q in a fetus with Down syndromeS Yakut, C Sanhal, E Manguoglu, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13)Z Cetin, E Mihci, I Keser, et al.
Andrologia|January 30, 2014
Ring chromosome 21 and monosomy 21 mosaicism in a patient with azoospermiaZ Cetin, O Altiok-Clark, M Sevuk, et al.
Journal of Investigational Allergology & Clinical Immunology|February 12, 2015
Selective IgM deficiency in a boy with ring chromosome 18F Celmeli, D Turkkahraman, Z Cetin, et al.
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
A PATIENT WITH AZOOSPERMIA AND 45,X/46,X,r(Y) (p11.2q11.2) MOSAICISM WITHOUT AZF DELETIONSO Altiok Clark, I Türker Köksal, S Berker Karaüzüm, et al.
Genetic Counseling (Geneva, Switzerland)|February 21, 2014
Prenatal diagnosis of isolated ventriculomegaly as a second trimester manifestation of de novo terminal 6q25 deletionZ 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 SyndromeZ Cetin, C Sanhal, S B Karauzum, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocationZ Cetin, E Mihci, I Keser, 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 literatureZ Cetin, E Mihci, S Yakut, 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.
Pageof 3