whole exome sequencing trang 4 tải miễn phí từ tailieuXANH

"whole exome sequencing" trang 4 - tải miễn phí từ tailieuXANH

Frequent variations in cancer-related genes may play prognostic role in treatment of patients with chronic myeloid leukemia

Frequent variations in cancer-related genes may play prognostic role in treatment of patients with chronic myeloid leukemia

6 2 1

Prenatal findings in a fetus with X-linked recessive type of chondrodysplasia punctata (CDPX1): A case report with novel mutation

Prenatal findings in a fetus with X-linked recessive type of chondrodysplasia punctata (CDPX1): A case report with novel mutation

6 76 0

An unusual hematopoietic stem cell transplantation for donor acute lymphoblastic leukemia: A case report

An unusual hematopoietic stem cell transplantation for donor acute lymphoblastic leukemia: A case report

5 52 0

TP53 and PTEN mutations were shared in concurrent germ cell tumor and acute megakaryoblastic leukemia

TP53 and PTEN mutations were shared in concurrent germ cell tumor and acute megakaryoblastic leukemia

8 67 0

Identification of p.HIS119LEU mutation in the G6PC gene of a Vietnamese patient with glycogen storage disease type Ia

Identification of p.HIS119LEU mutation in the G6PC gene of a Vietnamese patient with glycogen storage disease type Ia

8 82 0

Germline variation networks in the PI3K/ AKT pathway corresponding to familial high-incidence lung cancer pedigrees

Germline variation networks in the PI3K/ AKT pathway corresponding to familial high-incidence lung cancer pedigrees

10 46 1

Genomic signature of MTOR could be an immunogenicity marker in human colorectal cancer

Genomic signature of MTOR could be an immunogenicity marker in human colorectal cancer

21 22 1

Phenotypic Heterogeneity in a DFNA20/26 family segregating a novel ACTG1 mutation

Phenotypic Heterogeneity in a DFNA20/26 family segregating a novel ACTG1 mutation

11 2 1

Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes

Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes

9 71 0

Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes

Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes

13 29 2

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