Published in Turk J Pediatr on July 22, 1980
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Two genes are responsible for Griscelli syndrome at the same 15q21 locus. Genomics (2000) 1.54
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A case of Pearson syndrome associated with multiple renal cysts. Pediatr Nephrol (1996) 1.10
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Delayed-onset profound biotinidase deficiency. J Pediatr (1998) 0.96
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Neonatal tumor necrosis factor, interleukin-1 alpha, interleukin-1 beta, and interleukin-6 response to infection. Am J Perinatol (1994) 0.95
Impaired IgG antibody production to pneumococcal polysaccharides in patients with ataxia-telangiectasia. J Clin Immunol (1999) 0.93
Identification of ATM mutations using extended RT-PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A-T mutations in Israel. Hum Mutat (1998) 0.92
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The alterations of whole saliva constituents in patients with diabetes mellitus. Aust Dent J (1996) 0.91
Fanconi's aplastic anemia, analysis of 18 cases. Acta Haematol (1980) 0.91
The use of IgM-enriched intravenous immunoglobulin for the treatment of neonatal sepsis in preterm infants. Turk J Pediatr (1994) 0.90
A case of chronic severe neutropenia: oral findings and consequences of short-term granulocyte colony-stimulating factor treatment. Aust Dent J (1998) 0.89
The effect of zinc-supplemented bread consumption on school children with asymptomatic zinc deficiency. J Pediatr Gastroenterol Nutr (1998) 0.89
Familial Behçet's disease. Eur J Med (1992) 0.89
Neutrophil chemotaxis and periodontal status in Down's syndrome patients. J Nihon Univ Sch Dent (1993) 0.88
Clinical and immunological studies in a case of selective complete C1q deficiency. Clin Exp Immunol (1979) 0.88
Congenital erythropoietic porphyria successfully treated by allogeneic bone marrow transplantation. Blood (1998) 0.87
Cellular immunity in children with acute rheumatic fever and rheumatic carditis. Pediatr Res (1979) 0.87
Plasma amino acid response in young men given diets devoid of single essential amino acids. J Nutr (1972) 0.87
Type I hereditary tyrosinaemia: presentation of 11 cases. J Inherit Metab Dis (1991) 0.86
Mutations of chronic granulomatous disease in Turkish families. Eur J Clin Invest (2007) 0.86
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Ataxia-telangiectasia and xeroderma pigmentosum: no evidence of linkage to HLA. Tissue Antigens (1980) 0.86
Novel mutations cause biotinidase deficiency in Turkish children. J Inherit Metab Dis (2000) 0.86
The gingival crevicular fluid interleukin-1 beta and tumour necrosis factor-alpha levels in patients with rapidly progressive periodontitis. Aust Dent J (1995) 0.85
Human T-cell receptor CD3-epsilon (CD3E)/TaqI DNA polymorphism. Nucleic Acids Res (1989) 0.85
Screening for congenital hypothyroidism in Turkey. Eur J Pediatr (1995) 0.85
Tay-Sachs disease: a case report. Turk J Pediatr (1995) 0.85
The major presenting symptom in a biotinidase-deficient patient: laryngeal stridor. J Inherit Metab Dis (1992) 0.84
Molecular analysis of an MHC class II deficiency patient reveals a novel mutation in the RFX5 gene. Immunogenetics (1999) 0.84
Study of 12 mutations in Turkish cystic fibrosis patients. Hum Hered (1995) 0.84
Inborn errors of biotin metabolism. Clinical and laboratory features of eight cases. Turk J Pediatr (1995) 0.84
Neonatal tuberculosis. Pediatr Pathol (1993) 0.84
A case of Hartnup disorder with hypoalbuminemia and edema. Turk J Pediatr (1979) 0.83
Plasma amino acid response curve and amino acid requirements in young men: valine and lysine. J Nutr (1972) 0.83
Oxidative stress and asymmetric dimethylarginine is independently associated with carotid intima media thickness in peritoneal dialysis patients. Am J Nephrol (2007) 0.83
Isovaleric acidemia. Clinical presentation of 6 cases. Turk J Pediatr (1998) 0.83
HLA antigens associated with Behçet's disease. Arch Dermatol (1977) 0.83
Mutational analysis of Turkish galactosaemia patients. J Inherit Metab Dis (1995) 0.82
Selective IgA deficiency with unusual features: development of common variable immunodeficiency, Sjögren's syndrome, autoimmune hemolytic anemia and immune thrombocytopenic purpura. Acta Paediatr Jpn (1995) 0.82