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VPS13D-based disease: Expansion of the clinical phenotype in two brothers and mutation diversity in the Turkish population

Revue neurologique, 2022-11, Vol.178 (9), p.907-913

2022

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Molecular and population genetic analyses of β‐Thalassemia in Turkey

American journal of hematology, 1998-03, Vol.57 (3), p.215-220

1998

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A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype

Neurogenetics, 2009-07, Vol.10 (3), p.271-273

2009

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An unusual familial dementia associated with G131V PRNP mutation

European journal of neurology, 2021-02, Vol.28 (2), p.377-380

2021

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History and Origin of β-Thalassemia in Turkey: Sequence Haplotype Diversity of β-Globin Genes

Human biology, 2001-10, Vol.73 (5), p.661-674

2001

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β-THALASSEMIA IN TURKEY: A REVIEW OF THE CLINICAL, EPIDEMIOLOGICAL, MOLECULAR, AND EVOLUTIONARY ASPECTS

Hemoglobin, 2001-01, Vol.25 (2), p.227-239

2001

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Genotype-phenotype analysis in HbS-beta-thalassemia

Human heredity, 1997-05, Vol.47 (3), p.161-164

1997

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The molecular basis of β-thalassemia in Turkey

Human genetics, 1992-05, Vol.89 (3), p.315-318

1992

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PRENATAL DIAGNOSIS OF β-THALASSAEMIA AND SICKLE CELL ANAEMIA IN TURKEY

Prenatal diagnosis, 1996-03, Vol.16 (3), p.252-258

1996

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HbS/beta(del)-thalassemia associated with high levels of hemoglobins A2 and F in a Turkish family

American journal of hematology, 1998-09, Vol.59 (1), p.83-86

1998

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Posthuman Pathogenesis: Contagion in Literature, Arts, and Media

1, 2023

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A novel 13 BP deletion in the 3'UTR of the β-globin gene causes β-Thalassemia in a Turkish patient

Hemoglobin, 1993-12, Vol.17 (6), p.551-555

1993

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Explaining the characteristics of lateral shower age of cosmic ray extensive air showers

Pramāṇa, 2022-06, Vol.96 (2), Article 92

2022

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Rare β-Thalassemia Mutation in a Turkish Patient: FSC-36/37 (-T)

Human biology, 1997-04, Vol.69 (2), p.263-267

1997

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Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project

PloS one, 2023-10, Vol.18 (10), p.e0292180

2023

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Rare β‐thalassemia mutation IVS‐II‐848 (C‐A) first reported in a Turkish cypriot family

American journal of hematology, 1997-04, Vol.54 (4), p.338-339

1997

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Identification of the Chinese IVS-II-654 (C→T) β-Thalassemia Mutation in an Immigrant Turkish Family: Recurrence or Migration?

Human biology, 1999-04, Vol.71 (2), p.295-302

1999

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A novel deletion in a Turkish β-thalassemia patient detected by DGGE and direct sequencing: FSC 22-24 (-7 bp)

Hemoglobin, 1993-08, Vol.17 (4), p.387-391

1993

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A rare mutation [IVS‐I‐130 (G‐A)] in a Turkish β‐thalassemia major patient

American journal of hematology, 2000-04, Vol.63 (4), p.223-225

2000

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HbS/βdel‐thalassemia associated with high levels of hemoglobins A2 and F in a Turkish family

American journal of hematology, 1998-09, Vol.59 (1), p.83-86

1998

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Two Rare Hemoglobin Variants in the Turkish Population (Hb G-Coushatta (B 22(B4) GLU-ALA and Hb J Iran (B 77 (EF1) HIS-ASP)

Turkish journal of haematology, 2000-03, Vol.17 (1), p.27-28

2000

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A C → T substitution at nt ― 101 in a conserved DNA sequence of the promotor region of the β-globin gene is associated with silent β-thalassemia

Blood, 1989-05, Vol.73 (6), p.1705-1711

1989

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Homozygous ß-Thalassemia Associated with Familial Mediterranean Fever in a Turkish Patient

Turkish journal of haematology, 2001-09, Vol.18 (3), p.195-197

2001

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Tauopathies: A Distinct Class of Neurodegenerative Diseases

Balkan journal of medical genetics, 2007-01, Vol.10 (2), p.3-14

2007

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VPS13D-based disease: Expansion of the clinical phenotype in two brothers and mutation diversity in the Turkish population

Molecular and population genetic analyses of β‐Thalassemia in Turkey

A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype

An unusual familial dementia associated with G131V PRNP mutation

History and Origin of β-Thalassemia in Turkey: Sequence Haplotype Diversity of β-Globin Genes

β-THALASSEMIA IN TURKEY: A REVIEW OF THE CLINICAL, EPIDEMIOLOGICAL, MOLECULAR, AND EVOLUTIONARY ASPECTS

Genotype-phenotype analysis in HbS-beta-thalassemia

The molecular basis of β-thalassemia in Turkey

PRENATAL DIAGNOSIS OF β-THALASSAEMIA AND SICKLE CELL ANAEMIA IN TURKEY

HbS/beta(del)-thalassemia associated with high levels of hemoglobins A2 and F in a Turkish family

Posthuman Pathogenesis: Contagion in Literature, Arts, and Media

A novel 13 BP deletion in the 3'UTR of the β-globin gene causes β-Thalassemia in a Turkish patient

Natural History, Phenotypic Spectrum, and Discriminative Features of Multisystemic RFC1 Disease

Explaining the characteristics of lateral shower age of cosmic ray extensive air showers

Rare β-Thalassemia Mutation in a Turkish Patient: FSC-36/37 (-T)

Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project

Rare β‐thalassemia mutation IVS‐II‐848 (C‐A) first reported in a Turkish cypriot family

Identification of the Chinese IVS-II-654 (C→T) β-Thalassemia Mutation in an Immigrant Turkish Family: Recurrence or Migration?

A novel deletion in a Turkish β-thalassemia patient detected by DGGE and direct sequencing: FSC 22-24 (-7 bp)

A rare mutation [IVS‐I‐130 (G‐A)] in a Turkish β‐thalassemia major patient

HbS/βdel‐thalassemia associated with high levels of hemoglobins A2 and F in a Turkish family

Two Rare Hemoglobin Variants in the Turkish Population (Hb G-Coushatta (B 22(B4) GLU-ALA and Hb J Iran (B 77 (EF1) HIS-ASP)

A C → T substitution at nt ― 101 in a conserved DNA sequence of the promotor region of the β-globin gene is associated with silent β-thalassemia

Homozygous ß-Thalassemia Associated with Familial Mediterranean Fever in a Turkish Patient

Tauopathies: A Distinct Class of Neurodegenerative Diseases

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