List of bibliographic references
Number of relevant bibliographic references: 8.
List of associated KwdEn.i
Nombre de
documents | Descripteur |
|---|
| 7 | Humans |
| 7 | Lymphedema (diagnosis) |
| 6 | Lymphedema (genetics) |
| 5 | Female |
| 4 | Child, Preschool |
| 4 | Infant |
| 4 | Male |
| 4 | Mutation |
| 4 | Phenotype |
| 3 | Child |
| 2 | Adolescent |
| 2 | Adult |
| 2 | Craniofacial Abnormalities (diagnosis) |
| 2 | Craniofacial Abnormalities (genetics) |
| 2 | Genetics |
| 2 | Infant, Newborn |
| 2 | Lymphedema |
| 2 | Lymphedema (congenital) |
| 2 | Vascular Endothelial Growth Factor Receptor-3 (genetics) |
| 1 | Abnormalities, Multiple (genetics) |
| 1 | Age of Onset |
| 1 | Algorithms |
| 1 | Amino Acid Substitution |
| 1 | Calcium-Binding Proteins (genetics) |
| 1 | Codon |
| 1 | Connexin 43 (genetics) |
| 1 | DNA Mutational Analysis |
| 1 | Diagnosis, Differential |
| 1 | Diseases in Twins (diagnosis) |
| 1 | Diseases in Twins (genetics) |
| 1 | Diseases in Twins (pathology) |
| 1 | Edema (pathology) |
| 1 | Exons |
| 1 | Eye Abnormalities (diagnosis) |
| 1 | Eye Abnormalities (genetics) |
| 1 | Eyelashes (abnormalities) |
| 1 | Fetus |
| 1 | Foot Deformities, Congenital (diagnosis) |
| 1 | Foot Deformities, Congenital (genetics) |
| 1 | Forkhead Transcription Factors (genetics) |
| 1 | Gene |
| 1 | Gene Frequency |
| 1 | Genes, Dominant |
| 1 | Genetic Linkage |
| 1 | Genetic Predisposition to Disease |
| 1 | Genital Diseases, Male (diagnosis) |
| 1 | Genital Diseases, Male (genetics) |
| 1 | High-Throughput Nucleotide Sequencing (methods) |
| 1 | Human |
| 1 | Hydrops Fetalis (diagnosis) |
| 1 | Hydrops Fetalis (genetics) |
| 1 | Identification |
| 1 | Lymphangiectasis, Intestinal (diagnosis) |
| 1 | Lymphangiectasis, Intestinal (genetics) |
| 1 | Lymphatic Abnormalities (diagnosis) |
| 1 | Lymphatic Abnormalities (genetics) |
| 1 | Lymphedema (classification) |
| 1 | Lymphedema (pathology) |
| 1 | Lymphoscintigraphy |
| 1 | Nucleotide sequence |
| 1 | Pedigree |
| 1 | Polymerase Chain Reaction |
| 1 | Sequence Analysis, DNA |
| 1 | Sequencing |
| 1 | Syndactyly (diagnosis) |
| 1 | Syndactyly (genetics) |
| 1 | Syndrome |
| 1 | Tooth Abnormalities (diagnosis) |
| 1 | Tooth Abnormalities (genetics) |
| 1 | Tumor Suppressor Proteins (genetics) |
| 1 | Twins, Monozygotic |
| 1 | Varicose Veins (pathology) |
| 1 | Vascular Endothelial Growth Factor C (genetics) |
| 1 | Vascular Endothelial Growth Factor Receptor-3 (chemistry) |
| 1 | Vascular endothelial growth factor receptor 3 |
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EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/UK/Analysis
HfdIndexSelect -h $EXPLOR_AREA/Data/UK/Analysis/Author.i -k "P. Ostergaard"
HfdIndexSelect -h $EXPLOR_AREA/Data/UK/Analysis/Author.i \
-Sk "P. Ostergaard" \
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}}
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