HematologySCI(E)PubMed2LETTERliug268@126.com; liujunxiusanyuan@sina.com; niegj@nanoctr.cn4203-2045
Thiamine-responsive megaloblastic anemia syndrome is an autosomal recessive disorder characterized b...
<p>The arrowheads indicated different genotypes. <b>A, C, E, G, I</b> and <b>K</b> were the Temp-shi...
Mutations in the beta-globin (β-globin) gene cause beta-thalassaemia (β-thalassaemia).The screening ...
Background/Aims: Thiamine-responsive megaloblastic anemia syndrome is a rare autosomal recessive dis...
OBJECTIVE: To determine causative mutations and clinical status of 7 previously unreported kindreds ...
Objective: To determine causative mutations and clinical status of 7 previously unreported kindreds ...
Reported here is a 2-year-old girl who was diagnosed to have thiamine-responsive megaloblastic anemi...
OBJECTIVE: To determine causative mutations and clinical status of 7 previously unreported kindred...
AbstractThiamine-responsive megaloblastic anemia (TRMA) is an autosomal recessive syndrome character...
Thiamine responsive megaloblastic anemia (TRMA) is an autosomal recessive disease caused by loss of ...
Background. Thiamine-responsive megaloblastic anemia syndrome (TRMA), also known as Rogers syndrome,...
Thiamine-responsive megaloblastic anemia (TRMA) or Rogers syndrome is a rare autosomal recessive dis...
Aim: Thiamine-responsive megaloblastic anaemia syndrome (TRMA) is the association of diabetes mellit...
Thiamine-responsive megaloblastic anemia syndrome is an autosomal recessive disorder characterized b...
Thiamine metabolism dysfunction syndrome 2 (THMD2) is a rare metabolic disorder caused by SLC19A3 mu...
Thiamine-responsive megaloblastic anemia syndrome is an autosomal recessive disorder characterized b...
<p>The arrowheads indicated different genotypes. <b>A, C, E, G, I</b> and <b>K</b> were the Temp-shi...
Mutations in the beta-globin (β-globin) gene cause beta-thalassaemia (β-thalassaemia).The screening ...
Background/Aims: Thiamine-responsive megaloblastic anemia syndrome is a rare autosomal recessive dis...
OBJECTIVE: To determine causative mutations and clinical status of 7 previously unreported kindreds ...
Objective: To determine causative mutations and clinical status of 7 previously unreported kindreds ...
Reported here is a 2-year-old girl who was diagnosed to have thiamine-responsive megaloblastic anemi...
OBJECTIVE: To determine causative mutations and clinical status of 7 previously unreported kindred...
AbstractThiamine-responsive megaloblastic anemia (TRMA) is an autosomal recessive syndrome character...
Thiamine responsive megaloblastic anemia (TRMA) is an autosomal recessive disease caused by loss of ...
Background. Thiamine-responsive megaloblastic anemia syndrome (TRMA), also known as Rogers syndrome,...
Thiamine-responsive megaloblastic anemia (TRMA) or Rogers syndrome is a rare autosomal recessive dis...
Aim: Thiamine-responsive megaloblastic anaemia syndrome (TRMA) is the association of diabetes mellit...
Thiamine-responsive megaloblastic anemia syndrome is an autosomal recessive disorder characterized b...
Thiamine metabolism dysfunction syndrome 2 (THMD2) is a rare metabolic disorder caused by SLC19A3 mu...
Thiamine-responsive megaloblastic anemia syndrome is an autosomal recessive disorder characterized b...
<p>The arrowheads indicated different genotypes. <b>A, C, E, G, I</b> and <b>K</b> were the Temp-shi...
Mutations in the beta-globin (β-globin) gene cause beta-thalassaemia (β-thalassaemia).The screening ...
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