"Clinical phenotype" trang 1 - tải miễn phí từ tailieuXANH
Stepwise lactate kinetics in critically ill patients: Prognostic, influencing factors, and clinical phenotype

Stepwise lactate kinetics in critically ill patients: Prognostic, influencing factors, and clinical phenotype
8    160    1
Clinical phenotype-based gene prioritization: An initial study using semantic similarity and the human phenotype ontology

Clinical phenotype-based gene prioritization: An initial study using semantic similarity and the human phenotype ontology
11    57    0
GenIO: A phenotype-genotype analysis web server for clinical genomics of rare diseases

GenIO: A phenotype-genotype analysis web server for clinical genomics of rare diseases
6    49    0
Báo cáo y học:

Báo cáo y học: " The TNFalpha gene relates to clinical phenotype in alpha-1-antitrypsin deficiency"
8    36    0
Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: A case report

Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: A case report
4    85    0
A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: A report of two cases

A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: A report of two cases
6    52    0
Lobular breast cancers lack the inverse relationship between ER/PR status and cell growth rate characteristic of ductal cancers in two independent patient cohorts: Implications for tumor biology and adjuvant therapy

Lobular breast cancers lack the inverse relationship between ER/PR status and cell growth rate characteristic of ductal cancers in two independent patient cohorts: Implications for tumor biology and adjuvant therapy
11    50    0
Mutation status coupled with RNAsequencing data can efficiently identify important non-significantly mutated genes serving as diagnostic biomarkers of endometrial cancer

Mutation status coupled with RNAsequencing data can efficiently identify important non-significantly mutated genes serving as diagnostic biomarkers of endometrial cancer
11    64    0
A biological network-based regularized artificial neural network model for robust phenotype prediction from gene expression data

A biological network-based regularized artificial neural network model for robust phenotype prediction from gene expression data
11    49    0
A methodology for exploring biomarker – phenotype associations: Application to flow cytometry data and systemic sclerosis clinical manifestations

A methodology for exploring biomarker – phenotype associations: Application to flow cytometry data and systemic sclerosis clinical manifestations
15    46    0
Total knee arthroplasty according to the original knee phenotypes with kinematic alignment surgical technique-early clinical and functional outcomes

Total knee arthroplasty according to the original knee phenotypes with kinematic alignment surgical technique-early clinical and functional outcomes
10    69    0
Comparison of orthopaedic manifestations of multiple epiphyseal dysplasia caused by MATN3 versus COMP mutations: A case control study

Comparison of orthopaedic manifestations of multiple epiphyseal dysplasia caused by MATN3 versus COMP mutations: A case control study
8    55    1
Cox regression increases power to detect genotype-phenotype associations in genomic studies using the electronic health record

Cox regression increases power to detect genotype-phenotype associations in genomic studies using the electronic health record
7    134    2
Mutational and clinical analysis of the ENG gene in patients with pulmonary arterial hypertension

Mutational and clinical analysis of the ENG gene in patients with pulmonary arterial hypertension
12    2    1
Clinical and genetic characteristics of patients with fatty acid oxidation disorders identified by newborn screening

Clinical and genetic characteristics of patients with fatty acid oxidation disorders identified by newborn screening
7    45    0
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