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Turkish population-based screening for first identified changes of BRCA1 and BRCA2 genes in breast and/or ovarian cancer patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00525-2
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- Article
Chromosome Abnormalities Identified in 457 Spontaneous Abortions and Their Histopathological Findings.
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- Turkish Journal of Pathology, 2015, v. 31, n. 2, p. 111, doi. 10.5146/tjpath.2015.01303
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- Article
Rare Structural Chromosomal Abnormalities in Prenatal Diagnosis; Clinical and Cytogenetic Findings on 10125 Prenatal Cases.
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- Turkish Journal of Pathology, 2015, v. 31, n. 1, p. 36, doi. 10.5146/tjpath.2014.01280
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- Article
Mitochondrial ATPase Subunit 6 and Cytochrome B Gene Variations in Obese Turkish Children.
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- Journal of Clinical Research in Pediatric Endocrinology, 2014, v. 6, n. 4, p. 209, doi. 10.4274/jcrpe.1601
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- Article
The association of Klinefelter syndrome and multiple pterygium syndrome: an unusual presentation.
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- Turkish Journal of Pediatrics, 2013, v. 55, n. 5, p. 559
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- Article
Glikojen depo hastalığı tip III tanılı 10 Türk olgunun mutasyon analizleri: dört yeni mutasyonun tanımlanması.
- Published in:
- Türk Pediatri Arşivi, 2012, v. 47, n. 4, p. 278, doi. 10.4274/tpa.838
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- Article
Mutational analysis of ten Turkish patients with glycogen storage disease type III: identification of four novel mutations.
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- 2012
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- Journal Article
Pulmonary Alveolar Microlithiasis with Homozygous c.316G>C (p.G106R) Mutation: A case Report.
- Published in:
- 2012
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- Case Study
Screening of the HFE Gene Mutations in Turkish Patients with Cryptogenic Cirrhosis and Hemochromatosis.
- Published in:
- Turkiye Klinikleri Journal of Medical Sciences, 2010, v. 30, n. 6, p. 1891
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- Publication type:
- Article
Screening of the HFE gene mutations in Turkish patients with cryptogenic cirrhosis and hemochromatosis.
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- 2010
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- Publication type:
- Journal Article
Abnormal hemoglobins associated with the beta-globin gene in Antalya province, Turkey.
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- Turkish Journal of Medical Sciences, 2010, v. 40, n. 1, p. 127, doi. 10.3906/sag-0810-4
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- Article
Subtelomeric rearrangements of dysmorphic children with idiopathic mental retardation reveal 8 different chromosomal anomalies.
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- Turkish Journal of Pediatrics, 2009, v. 51, n. 5, p. 453
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- Article
Aplasia cutis congenita: three cases with three different underlying etiologies.
- Published in:
- Turkish Journal of Pediatrics, 2009, v. 51, n. 5, p. 510
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- Publication type:
- Article
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.
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- Human Mutation, 2007, v. 28, n. 10, p. 1014, doi. 10.1002/humu.20556
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- Article
Prenatal Diagnosis of b-Thalassemia in the Antalya Province.
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- Turkish Journal of Medical Sciences, 2005, v. 35, n. 4, p. 253
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- Publication type:
- Article
Germline mutations in the BRCA1 and BRCA2 genes in Turkish breast/ovarian cancer patientsCommunicated by Mark H. PaalmanOnline Citation: Human Mutation, Mutation in Brief #590 (2002) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/590.pdf
- Published in:
- Human Mutation, 2003, v. 21, n. 4, p. 444, doi. 10.1002/humu.9119
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- Publication type:
- Article
Germline mutations in the BRCA1 and BRCA2 genes in Turkish breast/ovarian cancer patients (Communicated by Mark H. Paalman) Online Citation: Human Mutation, Mutation in Brief #590 (2002) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/590.pdf)
- Published in:
- Human Mutation, 2003, v. 21, n. 4, p. 444, doi. 10.1002/humu.9119
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- Publication type:
- Article
Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome.
- Published in:
- Nature Genetics, 2002, v. 31, n. 4, p. 435, doi. 10.1038/ng935
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- Publication type:
- Article
Netherton Syndrome Associated with Idiopathic Congenital Hemihypertrophy.
- Published in:
- Pediatric Dermatology, 2002, v. 19, n. 4, p. 345, doi. 10.1046/j.1525-1470.2002.00098.x
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- Publication type:
- Article
Maternal Serum Screening for Down's Syndrome, Open Neural Tube Defects and Trisomy 18.
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- Clinical Chemistry & Laboratory Medicine, 2001, v. 39, n. 6, p. 487
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- Publication type:
- Article
The Effect of Hydroxyurea on Rabbit Subconjunctival Fibroblast Culture and Use of Hydroxyurea in Rabbits after Glaucoma Filtration Surgery.
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- Ophthalmologica, 1999, v. 213, n. 5, p. 311, doi. 10.1159/000027445
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- Publication type:
- Article
Nucleotide changes in the γ-globin promoter and the (AT)<sub>x</sub>N<sub>y</sub>(AT)<sub>z</sub> polymorphic sequence of βLCRHS-2 region associated with altered levels of HbF.
- Published in:
- European Journal of Human Genetics, 1999, v. 7, n. 3, p. 345, doi. 10.1038/sj.ejhg.5200284
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- Publication type:
- Article
Cytogenetic Study in 102 Infertile Men.
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- Urologia Internationalis, 1998, v. 61, n. 1, p. 32, doi. 10.1159/000030280
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- Article
Bloom's syndrome in a Turkish individual.
- Published in:
- Clinical Genetics, 1996, v. 49, n. 6, p. 314, doi. 10.1111/j.1399-0004.1996.tb03796.x
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- Publication type:
- Article
Monosomy 7 Myelodysplasia in Childhood.
- Published in:
- Acta Haematologica, 1994, v. 92, n. 1, p. 36, doi. 10.1159/000204135
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- Publication type:
- Article