List of bibliographic references
Number of relevant bibliographic references: 12.
List of associated KwdEn.i
Nombre de
documents | Descripteur |
|---|
| 8 | Humans |
| 5 | Adult |
| 5 | Female |
| 5 | Male |
| 4 | Adolescent |
| 4 | Child |
| 4 | Lymphedema (genetics) |
| 4 | Phenotype |
| 3 | Animals |
| 3 | Mutation |
| 2 | Child, Preschool |
| 2 | Lymphatic Vessels (pathology) |
| 2 | Lymphoscintigraphy |
| 2 | Vascular Endothelial Growth Factor Receptor-3 (genetics) |
| 1 | Anemia, Hemolytic, Congenital (genetics) |
| 1 | Biomarkers (analysis) |
| 1 | Blotting, Western |
| 1 | Cohort Studies |
| 1 | Craniofacial Abnormalities (diagnostic imaging) |
| 1 | Craniofacial Abnormalities (genetics) |
| 1 | Databases, Genetic |
| 1 | Ectodermal Dysplasia (diagnosis) |
| 1 | Edema (diagnosis) |
| 1 | Edema (genetics) |
| 1 | Endothelium, Lymphatic (immunology) |
| 1 | Endothelium, Lymphatic (metabolism) |
| 1 | Endothelium, Lymphatic (pathology) |
| 1 | Facies |
| 1 | Failure to Thrive (diagnosis) |
| 1 | Family |
| 1 | Family Health |
| 1 | Frameshift Mutation (genetics) |
| 1 | Genetic Association Studies |
| 1 | Genetic Predisposition to Disease (genetics) |
| 1 | Granuloma (complications) |
| 1 | Granuloma (pathology) |
| 1 | Heart Defects, Congenital (diagnosis) |
| 1 | Heterozygote |
| 1 | Homeodomain Proteins (metabolism) |
| 1 | Hydrops Fetalis (genetics) |
| 1 | Infant, Newborn |
| 1 | Intellectual Disability (genetics) |
| 1 | Ion Channels (genetics) |
| 1 | Kinesin (genetics) |
| 1 | Lymphangiectasis, Intestinal (diagnostic imaging) |
| 1 | Lymphangiectasis, Intestinal (genetics) |
| 1 | Lymphangiogenesis (immunology) |
| 1 | Lymphatic System (diagnostic imaging) |
| 1 | Lymphatic System (pathology) |
| 1 | Lymphatic Vessels (immunology) |
| 1 | Lymphedema (congenital) |
| 1 | Lymphedema (diagnostic imaging) |
| 1 | Lymphedema (etiology) |
| 1 | Lymphedema (pathology) |
| 1 | Mice |
| 1 | Microcephaly (genetics) |
| 1 | Middle Aged |
| 1 | Noonan Syndrome (diagnosis) |
| 1 | Pedigree |
| 1 | Penetrance |
| 1 | Retinal Diseases (genetics) |
| 1 | Scrotum (pathology) |
| 1 | Sequence Analysis, DNA |
| 1 | Turner Syndrome (diagnosis) |
| 1 | Turner Syndrome (genetics) |
| 1 | Vascular Endothelial Growth Factor C (genetics) |
| 1 | Vesicular Transport Proteins (metabolism) |
| 1 | Young Adult |
| 1 | Zebrafish |
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/UK/Analysis
HfdIndexSelect -h $EXPLOR_AREA/Data/UK/Analysis/Author.i -k "Kristiana Gordon"
HfdIndexSelect -h $EXPLOR_AREA/Data/UK/Analysis/Author.i \
-Sk "Kristiana Gordon" \
| HfdSelect -Kh $EXPLOR_AREA/Data/UK/Analysis/biblio.hfd
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|wiki= Wicri/Sante
|area= LymphedemaV1
|flux= UK
|étape= Analysis
|type= indexItem
|index= Author.i
|clé= Kristiana Gordon
}}
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