Tuna Gulten

Bursa, 16059, Turkey

Last Updated: 09/26/2026

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Found 13 publications

Dyskeratosis Congenita: A Case Report.

Dyskeratosis Congenita: A Case Report.

Journal: Genetic counseling (Geneva, Switzerland)

Published: January 01, 2016

Spectrum of EGFR gene mutations and ALK rearrangements in lung cancer patients in Turkey.

Spectrum of EGFR gene mutations and ALK rearrangements in lung cancer patients in Turkey.

Journal: SpringerPlus

Published: October 28, 2015

MULTIPLE CONGENITAL ANOMALIES IN A CHILD WITH 47,XY,+der(8;9)(p10;p10): A CASE REPORT.

MULTIPLE CONGENITAL ANOMALIES IN A CHILD WITH 47,XY,+der(8;9)(p10;p10): A CASE REPORT.

Journal: Genetic counseling (Geneva, Switzerland)

Published: September 10, 2015

TURNER SYNDROME WITH 45,X/46,X,I(Xq)/47,X,I(Xq),I(Xq) KARYOTYPE.

TURNER SYNDROME WITH 45,X/46,X,I(Xq)/47,X,I(Xq),I(Xq) KARYOTYPE.

Journal: Genetic counseling (Geneva, Switzerland)

Published: September 10, 2015

A NOVEL MUTATION IN NPR2 GENE IN A PATIENT WITH ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE.

A NOVEL MUTATION IN NPR2 GENE IN A PATIENT WITH ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE.

Journal: Genetic counseling (Geneva, Switzerland)

Published: September 10, 2015

Qualitative and quantitative evaluation of the BCR-ABL fusion gene in chronic myelogenous leukemia by flourescence in situ hybridization and molecular genetic methods.

Qualitative and quantitative evaluation of the BCR-ABL fusion gene in chronic myelogenous leukemia by flourescence in situ hybridization and molecular genetic methods.

Journal: Genetic testing and molecular biomarkers

Published: August 27, 2015

A novel mutation in the FRAS1 gene in a patient with Fraser syndrome.

A novel mutation in the FRAS1 gene in a patient with Fraser syndrome.

Journal: Genetic counseling (Geneva, Switzerland)

Published: June 06, 2015

A fertile patient with 45X/47XXX mosaicism.

A fertile patient with 45X/47XXX mosaicism.

Journal: Genetic counseling (Geneva, Switzerland)

Published: June 06, 2015

Association of the ACE I/D gene polymorphisms with JAK2V617F-positive polycythemia vera and essential thrombocythemia.

Association of the ACE I/D gene polymorphisms with JAK2V617F-positive polycythemia vera and essential thrombocythemia.

Journal: Genetic testing and molecular biomarkers

Published: May 09, 2015

MMP2 gene-735 C/T and MMP9 gene -1562 C/T polymorphisms in JAK2V617F positive myeloproliferative disorders.

MMP2 gene-735 C/T and MMP9 gene -1562 C/T polymorphisms in JAK2V617F positive myeloproliferative disorders.

Journal: Asian Pacific journal of cancer prevention : APJCP

Published: February 17, 2015

De novo partial trisomy distal 4q: a case report.

De novo partial trisomy distal 4q: a case report.

Journal: Genetic counseling (Geneva, Switzerland)

Published: January 01, 2014

Another small supernumerary marker chromosome derived from chromosome 9 in a Klinefelter patient.

Another small supernumerary marker chromosome derived from chromosome 9 in a Klinefelter patient.

Journal: The West Indian medical journal

Published: September 12, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026