Found: 24
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Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Previously Unreported Chromosomal Aberrations of t(3;3)(q29;q23), t(4;11)(q21;q23), and t(11;18)(q10;q10) in a Patient with Accelerated Phase Ph+ CML.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
A familial interstitial 4q35 deletion with no discernible clinical effects.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 8, p. 1836, doi. 10.1002/ajmg.a.37097
- By:
- Publication type:
- Article
Molecular diagnosis of hematological malignancies by RT-PCR.
- Published in:
- Turkish Journal of Cancer, 2005, v. 35, n. 3, p. 113
- By:
- Publication type:
- Article
Sensorimotor polyneuropathy in patients with SMA type-1: Electroneuromyographic findings.
- Published in:
- Muscle & Nerve, 2013, v. 48, n. 1, p. 117, doi. 10.1002/mus.23722
- By:
- Publication type:
- Article
Progesterone may be a regulator and B12 could be an indicator of the proximal D4Z4 repeat methylation status on 4q35ter.
- Published in:
- Journal of Neurochemistry, 2024, v. 168, n. 9, p. 3209, doi. 10.1111/jnc.16196
- By:
- Publication type:
- Article
Clinical expression of familial Williams-Beuren syndrome in a Turkish family.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 1/2, p. 153, doi. 10.1515/jpem-2013-0167
- By:
- Publication type:
- Article
Differential PTEN Protein Expression Profiles in Superficial versus Invasive Bladder Cancers.
- Published in:
- Urologia Internationalis, 2005, v. 75, n. 2, p. 102, doi. 10.1159/000085933
- By:
- Publication type:
- Article
Estradiol differentially regulates DUX4, β-catenin and PAX3/PAX7 in primary myoblasts of facioscapulohumeral muscular dystrophy patients.
- Published in:
- Turkish Journal of Biochemistry / Turk Biyokimya Dergisi, 2021, v. 46, n. 4, p. 435, doi. 10.1515/tjb-2020-0351
- By:
- Publication type:
- Article
Celiac disease in patients with Williams-Beuren syndrome.
- Published in:
- Turkish Journal of Pediatrics, 2015, v. 57, n. 6, p. 599
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- Publication type:
- Article
Subtelomeric rearrangements of dysmorphic children with idiopathic mental retardation reveal 8 different chromosomal anomalies.
- Published in:
- Turkish Journal of Pediatrics, 2009, v. 51, n. 5, p. 453
- By:
- Publication type:
- Article
Loss of Y Chromosome in Bone Marrow Cells with Hematologic Malignancies: A Retrospective Study.
- Published in:
- UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi, 2023, v. 33, n. 4, p. 221, doi. 10.4999/uhod.237227
- By:
- Publication type:
- Article
Real-Life Experience of Dose-Adjusted Venetoclax in Acute Myeloid Leukemia Patients Concomitantly Using Posaconazole for Antifungal Prophylaxis: A Single-Center Experience.
- Published in:
- UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi, 2023, v. 33, n. 2, p. 75, doi. 10.4999/uhod.236880
- By:
- Publication type:
- Article
Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 2, p. 349, doi. 10.1002/ajmg.a.33811
- By:
- Publication type:
- Article
The value of donor lymphocyte infusions in thalassemia patients at imminent risk of graft rejection following stem cell transplantation.
- Published in:
- Pediatric Blood & Cancer, 2012, v. 58, n. 3, p. 453, doi. 10.1002/pbc.23350
- By:
- Publication type:
- Article
KRONİK MİYELOİD LÖSEMİDE TANI ANINDA İLAVE KROMOZOMAL ABNORMALİTELER VE VARYANT PHİLADEPHİA TRANSLOKASYONLARI; TEK MERKEZ DENEYİMİ.
- Published in:
- Medical Journal of Suleyman Demirel University, 2019, v. 26, n. 3, p. 320, doi. 10.17343/sdutfd.535002
- By:
- Publication type:
- Article
A Novel Coincidence: Essential Thrombocythemia with Facioscapulohumeral Muscular Dystrophy.
- Published in:
- Turkish Journal of Hematology, 2020, v. 37, n. 4, p. 306, doi. 10.4274/tjh.galenos.2020.2020.0363
- By:
- Publication type:
- Article
The Coexistence of Chronic Lymphocytic Leukemia and Multiple Myeloma.
- Published in:
- Turkish Journal of Hematology, 2019, v. 36, n. 2, p. 124, doi. 10.4274/tjh.galenos.2018.2018.0096
- By:
- Publication type:
- Article
Investigation of MDM2 Oncogene Copy Number Alterations in Cases of Chronic Lymphocytic Leukemia.
- Published in:
- Turkish Journal of Hematology, 2019, v. 36, n. 2, p. 126, doi. 10.4274/tjh.galenos.2018.2018.0270
- By:
- Publication type:
- Article
Coexistence of a Homozygous Chromosome 4q35.2 Deletion and Hidden IQSEC2 Pathogenic Variant in a Child with Intellectual Disability.
- Published in:
- Cytogenetic & Genome Research, 2021, v. 161, n. 3/4, p. 153, doi. 10.1159/000515368
- By:
- Publication type:
- Article
Evaluation of PTEN and Mcl-1 expressions in NSCLC expressing wild-type or mutated EGFR.
- Published in:
- Medical Oncology, 2010, v. 27, n. 3, p. 853, doi. 10.1007/s12032-009-9296-7
- By:
- Publication type:
- Article
Analysis of DUX4 Expression in Bone Marrow and Re-Discussion of DUX4 Function in the Health and Disease.
- Published in:
- Turkish Journal of Pathology, 2022, v. 38, n. 3, p. 219, doi. 10.5146/tjpath.2021.01564
- By:
- Publication type:
- Article
Rare Structural Chromosomal Abnormalities in Prenatal Diagnosis; Clinical and Cytogenetic Findings on 10125 Prenatal Cases.
- Published in:
- Turkish Journal of Pathology, 2015, v. 31, n. 1, p. 36, doi. 10.5146/tjpath.2014.01280
- By:
- Publication type:
- Article
Coexistence of deletion, ring, and monosomy of chromosome 7 in a patient with MDS-RAEB-2.
- Published in:
- Eastern Journal of Medicine, 2018, v. 23, n. 4, p. 328, doi. 10.5505/ejm.2018.65487
- By:
- Publication type:
- Article