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Altuğ Koç

Showing results (1-10 of 30) with videos related to

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Noro Psikiyatri Arsivi|September 11, 2024
Imagawa-Matsumoto Syndrome: The First Case From TurkeyZeliha Yücel, Emine Berrin Yüksel, Altuğ Koç
Balkan Medical Journal|September 22, 2018
Targeted Next-Generation Sequencing of <i>MLH1, MSH2</i>, and <i>MSH6</i> Genes in Patients with Endometrial Carcinoma under 50 Years of AgeTaha Reşid Özdemir, Murat Alan, Muzaffer Sancı, et al.
Asian Journal of Andrology|August 25, 2009
Supernumerary marker chromosome 15 in a male with azoospermia and open bite deformityAltuğ Koç, S Odül Onur, Mehmet Ali Ergün, et al.
Turk Kardiyoloji Dernegi Arsivi : Turk Kardiyoloji Derneginin Yayin Organidir|March 20, 2014
Antenatal diagnosis of left atrial isomerism and heterotaxy syndrome in fetus with Meckel-Gruber syndromeSeçil Kurtulmuş, Savaş Demirpençe, Deniz Can Öztekin, et al.
Cytogenetic and Genome Research|June 30, 2020
Warburg Micro Syndrome 1 due to Segmental Paternal Uniparental Isodisomy of Chromosome 2 Detected by Whole-Exome Sequencing and Homozygosity MappingAbdullah Sezer, Gülsüm Kayhan, Altuğ Koç, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2022
Late onset Bartter syndrome: Bartter syndrome type 2 presenting with isolated nephrocalcinosis and high parathyroid hormone levels mimicking primary hyperparathyroidismGizem Yıldız, Meral Torun Bayram, Tayfun Çinleti, et al.
American Journal of Medical Genetics. Part A|June 12, 2025
Prenatal Diagnosis of HSPG2-Related Dyssegmental Dysplasia: The First Report From TurkeyMehmet Berkay Akcan, Raziye Torun, Tuba Sözen Türk, et al.
Hormones (Athens, Greece)|February 20, 2019
A toddler with a novel LEPR mutationCoşkun Armağan, Ceren Yılmaz, Altuğ Koç, et al.
The Turkish Journal of Pediatrics|July 31, 2008
A case with a ring chromosome 22Altuğ Koç, Kadri Karaer, Mehmet Ali Ergün, et al.
The Journal of Obstetrics and Gynaecology Research|February 13, 2010
Prenatal diagnosis of mosaic ring 22 duplication/deletion with terminal 22q13 deletion due to abnormal first trimester screening and choroid plexus cyst detected on ultrasoundAltuğ Koç, Ozgür Arisoy, Elif Pala, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Noro Psikiyatri Arsivi|September 11, 2024
Imagawa-Matsumoto Syndrome: The First Case From TurkeyZeliha Yücel, Emine Berrin Yüksel, Altuğ Koç
Balkan Medical Journal|September 22, 2018
Targeted Next-Generation Sequencing of <i>MLH1, MSH2</i>, and <i>MSH6</i> Genes in Patients with Endometrial Carcinoma under 50 Years of AgeTaha Reşid Özdemir, Murat Alan, Muzaffer Sancı, et al.
Asian Journal of Andrology|August 25, 2009
Supernumerary marker chromosome 15 in a male with azoospermia and open bite deformityAltuğ Koç, S Odül Onur, Mehmet Ali Ergün, et al.
Turk Kardiyoloji Dernegi Arsivi : Turk Kardiyoloji Derneginin Yayin Organidir|March 20, 2014
Antenatal diagnosis of left atrial isomerism and heterotaxy syndrome in fetus with Meckel-Gruber syndromeSeçil Kurtulmuş, Savaş Demirpençe, Deniz Can Öztekin, et al.
Cytogenetic and Genome Research|June 30, 2020
Warburg Micro Syndrome 1 due to Segmental Paternal Uniparental Isodisomy of Chromosome 2 Detected by Whole-Exome Sequencing and Homozygosity MappingAbdullah Sezer, Gülsüm Kayhan, Altuğ Koç, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2022
Late onset Bartter syndrome: Bartter syndrome type 2 presenting with isolated nephrocalcinosis and high parathyroid hormone levels mimicking primary hyperparathyroidismGizem Yıldız, Meral Torun Bayram, Tayfun Çinleti, et al.
American Journal of Medical Genetics. Part A|June 12, 2025
Prenatal Diagnosis of HSPG2-Related Dyssegmental Dysplasia: The First Report From TurkeyMehmet Berkay Akcan, Raziye Torun, Tuba Sözen Türk, et al.
Hormones (Athens, Greece)|February 20, 2019
A toddler with a novel LEPR mutationCoşkun Armağan, Ceren Yılmaz, Altuğ Koç, et al.
The Turkish Journal of Pediatrics|July 31, 2008
A case with a ring chromosome 22Altuğ Koç, Kadri Karaer, Mehmet Ali Ergün, et al.
The Journal of Obstetrics and Gynaecology Research|February 13, 2010
Prenatal diagnosis of mosaic ring 22 duplication/deletion with terminal 22q13 deletion due to abnormal first trimester screening and choroid plexus cyst detected on ultrasoundAltuğ Koç, Ozgür Arisoy, Elif Pala, et al.
Pageof 3