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Unexpected Coexistence of a Derivative t(21;21) and Complementary Mosaic r(21) in a Female with Multiple Miscarriages

Cytogenetic and genome research, 2019-08, Vol.158 (2), p.83-87

2019

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Fetal HLA-G alleles and their effect on miscarriage

Advances in clinical and experimental medicine : official organ Wroclaw Medical University, 2018-09, Vol.27 (9), p.1233-1237

2018

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Experiences in the molecular genetic and histopathological evaluation of calpainopathies

Neurogenetics, 2022-04, Vol.23 (2), p.103-114

2022

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Molecular genetic evaluation of NLRP3, MVK and TNFRSF1A associated periodic fever syndromes

International journal of immunogenetics, 2019-08, Vol.46 (4), p.232-240

2019

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cfDNA in exhaled breath condensate (EBC) and contamination by ambient air: toward volatile biopsies

Journal of breath research, 2019-05, Vol.13 (3), p.036006-036006

2019

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Targeted fetal cell‐free DNA screening for aneuploidies in 4,594 pregnancies: Single center study

Molecular genetics & genomic medicine, 2019-07, Vol.7 (7), p.e00678-n/a

2019

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The Efficiency of SNP-Based Microarrays in the Detection of Copy-Neutral Events at 15q11.2 and 11p15.5 Loci

Journal of pediatric genetics (Birmingham, Ala.), 2020-03, Vol.9 (1), p.009-018

2020

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Does Follicle-Stimulating hormone receptor polymorphism status affect In vitro fertilization-intracytoplasmic sperm injection results and live birth rate? A retrospective study

Journal of human reproductive sciences, 2022-01, Vol.15 (1), p.58-63

2022

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Impact of next‐generation sequencing panels in the evaluation of limb‐girdle muscular dystrophies

Annals of human genetics, 2019-09, Vol.83 (5), p.331-347

2019

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Clinical and genetic spectrum from a prototype of ciliopathy: Joubert syndrome

Clinical neurology and neurosurgery, 2023-01, Vol.224, p.107560-107560, Article 107560

2023

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Targeted next generation sequencing in patients with maturity-onset diabetes of the young (MODY)

Journal of pediatric endocrinology & metabolism : JPEM, 2018-12, Vol.31 (12), p.1295

2018

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Distinctively Different Phenotypes of Two Cases with a Rare Karyotype of 45,X/47,XYY Mosaicism: Case Report and Literature Review

The journal of pediatric research, 2022-12, Vol.9 (4), p.401-408

2022

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The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome

Turkish journal of pediatrics, 2019-07, Vol.61 (4), p.589-593

2019

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Can the Cell-free DNA Test Predict Placenta Accreta Spectrum or Placenta Previa Totalis?

Zeitschrift fur Geburtshilfe und Neonatologie, 2022-04, Vol.226 (2), p.92

2022

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The relation between distant metastasis and genetic change type in stage IV lung adenocarcinoma patients at diagnosis

The clinical respiratory journal, 2021-02, Vol.15 (2), p.196-202

2021

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Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with primary male infertility: A single-center study

Turkish journal of urology, 2020-03, Vol.46 (2), p.95-100

2020

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Assessment of Quality of Life of Chronic Myeloid Leukemia Patients by Using the EORTC QLQ-C30

Turkish journal of haematology, 2017-06, Vol.34 (2), p.197-199

2017

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First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss

Turkish archives of otorhinolaryngology, 2019-09, Vol.57 (3), p.140-148

2019

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The effect of progesterone supplementation in women with threatened miscarriage on fetal fraction in non-invasive prenatal testing: A matched case-control study

Journal of gynecology obstetrics and human reproduction, 2023-10, Vol.52 (8), p.102662-102662, Article 102662

2023

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Molecular genetic evaluation of NLRP 3, MVK and TNFRSF 1A associated periodic fever syndromes

International journal of immunogenetics, 2019-08, Vol.46 (4), p.232-240

2019

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QF-PCR in invasive prenatal diagnosis: a single-center experience in Turkey

Turkish journal of medical sciences, 2017-01, Vol.47 (1), p.142-147

2017

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Assessment of quality of life of chronic myeloid leukemia patients by using the EORTC QLQ-C30

Turkish journal of haematology, 2017, Vol.34 (2), p.197-199

2017

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Adolesan bir Erkek Çocukta Poliüri; Tanısal Güçlük

Turkish Journal of Pediatric Disease, 2021-03, p.1-4

2021

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The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome

The Turkish journal of pediatrics, 2019, Vol.61 (4), p.589-593

2019

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AN UNUSUAL CASE OF ACQUIRED PARTIAL LIPODYSTROPHY PRESENTING WITH ACANTHOSIS NIGRICANS

Acta endocrinologica (Bucharest, Romania : 2005), 2019-01, Vol.5 (1), p.129-130

2019

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Unexpected Coexistence of a Derivative t(21;21) and Complementary Mosaic r(21) in a Female with Multiple Miscarriages

Fetal HLA-G alleles and their effect on miscarriage

Experiences in the molecular genetic and histopathological evaluation of calpainopathies

Molecular genetic evaluation of NLRP3, MVK and TNFRSF1A associated periodic fever syndromes

cfDNA in exhaled breath condensate (EBC) and contamination by ambient air: toward volatile biopsies

Targeted fetal cell‐free DNA screening for aneuploidies in 4,594 pregnancies: Single center study

The Efficiency of SNP-Based Microarrays in the Detection of Copy-Neutral Events at 15q11.2 and 11p15.5 Loci

Does Follicle-Stimulating hormone receptor polymorphism status affect In vitro fertilization-intracytoplasmic sperm injection results and live birth rate? A retrospective study

Impact of next‐generation sequencing panels in the evaluation of limb‐girdle muscular dystrophies

Clinical and genetic spectrum from a prototype of ciliopathy: Joubert syndrome

Targeted next generation sequencing in patients with maturity-onset diabetes of the young (MODY)

Distinctively Different Phenotypes of Two Cases with a Rare Karyotype of 45,X/47,XYY Mosaicism: Case Report and Literature Review

The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome

Can the Cell-free DNA Test Predict Placenta Accreta Spectrum or Placenta Previa Totalis?

The relation between distant metastasis and genetic change type in stage IV lung adenocarcinoma patients at diagnosis

Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with primary male infertility: A single-center study

Assessment of Quality of Life of Chronic Myeloid Leukemia Patients by Using the EORTC QLQ-C30

First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss

The effect of progesterone supplementation in women with threatened miscarriage on fetal fraction in non-invasive prenatal testing: A matched case-control study

Molecular genetic evaluation of NLRP 3, MVK and TNFRSF 1A associated periodic fever syndromes

QF-PCR in invasive prenatal diagnosis: a single-center experience in Turkey

Assessment of quality of life of chronic myeloid leukemia patients by using the EORTC QLQ-C30

Adolesan bir Erkek Çocukta Poliüri; Tanısal Güçlük

The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome

AN UNUSUAL CASE OF ACQUIRED PARTIAL LIPODYSTROPHY PRESENTING WITH ACANTHOSIS NIGRICANS

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