Ç. Altay

发表

Prenatal diagnosis of sickle cell anemia using PCR and restriction enzyme Dde I.

S. Beksaç, A. Kutlar, A. Gürgey, 1993, The Turkish journal of pediatrics.

Anemia associated with diabetes mellitus.

A. Gürgey, Ç. Altay, N. Yordam,, 1995, Pediatric hematology and oncology.

Additional evidence for a deleted gene for serum alpha-1-antitrypsin.

N. Erdoğan, Ç. Altay, M. Fagerhol, 1973, The New England journal of medicine.

probes identification of the types by hybridization of amplified DNA with synthetic Mild and severe beta-thalassemia among homozygotes from Turkey:

A. Kutlar, Y. Kilinç, Ç. Altay, 2013 .

Role of protein C in childhood cerebrovascular occlusive accidents

B. Anlar, Ç. Altay, Ş. Kirazlı, 1989, European Journal of Pediatrics.

Evidence for the existence of the PAF acetylhydrolase mutation (Val279Phe) in non-Japanese populations: a preliminary study in Turkey, Azerbaijan, and Kyrgyzstan.

Ç. Altay, B. Tunç, A. Gurgey, 2001, Thrombosis research.

Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey.

A. Gürgey, Ç. Altay, A. Gurgey, 2000, Haematologica.

Prevalence of PAI‐1 gene 4G/5G genotype in Azerbaijan and Kyrgyzstan populations: literature review

Ç. Altay, A. Gurgey, G. Balta, 2003, Journal of thrombosis and haemostasis : JTH.

Plasma, erythrocyte, and leukocyte ascorbic acid concentrations in children with iron deficiency anemia.

Ç. Altay, B. Say, S. Donmez, 1975, The Journal of pediatrics.

CHRONIC HEMOLYTIC ANEMIA ASSOCIATED WITH GLUCOSE 6-PHOSPHATE DEHYDROGENASE (GUADALAJARA)1159 C → T (387 ARG → CYS) DEFICIENCY ASSOCIATED WITH GILBERT SYNDROME IN A TURKISH PATIENT

A. Gürgey, Ç. Altay, İ. Yenicesu, 2002, Pediatric hematology and oncology.

Clinical and haematological evaluation of beta thalassaemia intermedia with increased Hb F and Hb A2 in heterozygotes: beta thalassaemia intermedia I.

Ç. Altay, A. Gurgey, 1985, Journal of medical genetics.

Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetuses.

S. Beksaç, Ç. Altay, C. Kiefer, 1991, Journal of chromatography.

Malignant hyperthermia in a patient with sickle cell anemia.

A. Gürgey, Ç. Altay, S. Ozgen, 1989, Turkish Journal of Pediatrics.

Congenital hypoplastic anemia in six patients: unusual association of short proximal phalanges with mild anemia.

M. Çetin, G. Irken, A. Gürgey, 1995, Pediatric hematology and oncology.

Nitroblue tetrazolium test in children with malnutrition.

Ç. Altay, B. Say, A. Bingol, 1972, The Journal of pediatrics.

Pearson's marrow-pancreas syndrome in 2 Turkish children.

A. Rötig, A. Gürgey, Ç. Altay, 1992, Acta haematologica.

Importance of RDW value in differential diagnosis of hypochrome anemias

A. Gürgey, Ç. Altay, F. Gumruk, 2002, American journal of hematology.

Distribution of hemoglobinopathies in Turkey. Report based on studies conducted at the Hacettepe Children's Hospital and the reviews of other studies.

A. Gürgey, Ç. Altay, 1986, The Turkish journal of pediatrics.

The Factor V Leiden and Prothrombin G20210A Mutations in Kirghiz Population

Ç. Altay, M. Tuncer, A. Gurgey, 2000, Thrombosis and Haemostasis.

Prenatal diagnosis of hemoglobinopathies in Turkey: Hacettepe experience.

S. Beksaç, A. Gürgey, L. Mesci, 1996, Pediatric hematology and oncology.

Premarital screening of hemoglobinopathies: a pilot study in Turkey.

S. Beksaç, A. Gürgey, Ç. Altay, 1996, Human heredity.

Frequency of red cell adenosine deaminase and 6-phosphogluconate dehydrogenase in a sample of the Turkish population.

Ç. Altay, B. Say, E. Tuncbilek, 1974, Human Heredity.

Heterozygous β‐thalassemia: Relationship between the hematological phenotype and the type of β‐thalassemia mutation

Ç. Altay, A. Gurgey, Ç. Altay, 1993 .

β‐Thalassemia Intermedia in Turkey

A. Gürgey, Ç. Altay, 1990 .

Beta-thalassemia intermedia in Turkey.

A. Gürgey, Ç. Altay, 1990, Annals of the New York Academy of Sciences.