Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by J Traeger-Synodinos
CLINICAL AND HEMATOLOGICAL PHENOTYPE IN 9 FAMILIES WITH THE RARE Β-Gene C>G MUTATION AT Nt POSITION 6 3′ TO THE TERMINATION CODON. 119
Pediatric Research
Child Health
Pediatrics
Perinatology
Phenotype-Genotype Correlation of Haemoglobinopathy H Disease in Greece 31
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
Diagnostic Pitfall in PCR-Based -Thalassemia Genotyping Resulting From a (G->c) Polymorphism at Nucleotide 71 3' to the 2-Globin Gene Termination Codon
Clinical Chemistry
Biochemistry
Clinical Biochemistry
A Start Codon Mutation of the TSPAN12 Gene in Chinese Families Causes Clinical Heterogeneous Familial Exudative Vitreoretinopathy
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Identification of a Novel Mutation in the Β-Globin Gene 3′ Untranslated Region [+1,506 (A>C)] in a Japanese Male With a Heterozygous Β-Thalassemia Phenotype
Hemoglobin
Biochemistry
Genetics
Clinical Biochemistry
Hematology
Premature Termination Codon Mutations in the Von Willebrand Factor Gene Are Associated With Allele-Specific and Position-Dependent mRNA Decay
Haematologica
Hematology
Rare TACI Mutation in a 3-Year-Old Boy With CVID Phenotype
Frontiers in Pediatrics
Child Health
Pediatrics
Perinatology
A Premature-Termination Mutation in the Mus Musculus Cyclin-Dependent Kinase 3 Gene
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Mutations at Codon 974 of the DPYD Gene Are a Rare Event
British Journal of Cancer
Cancer Research
Oncology
Phenotype and Prognosis of the Lamin a/C Gene (LMNA) Mutation Carriers in Japan
Circulation Journal
Medicine
Cardiovascular Medicine
Cardiology
Β-Thalassemia Mutation at Codon 37 (TGG>>TGA) Detected in a Turkish Family
Turkish Journal of Haematology
Hematology
