List of bibliographic references
Number of relevant bibliographic references: 24.
[20-40] [
0 - 20][
0 - 24]
List of associated KwdEn.i
Nombre de
documents | Descripteur |
|---|
| 17 | Humans |
| 16 | Female |
| 14 | Male |
| 13 | Lymphedema (genetics) |
| 13 | Mutation |
| 9 | Child |
| 8 | Phenotype |
| 7 | Adolescent |
| 7 | Lymphedema |
| 6 | Adult |
| 6 | Child, Preschool |
| 5 | Infant, Newborn |
| 5 | Pedigree |
| 4 | Genetics |
| 4 | Lymphedema (congenital) |
| 3 | Facies |
| 3 | Genetic Linkage |
| 3 | Heterozygote |
| 3 | Infant |
| 3 | Kinesin (genetics) |
| 3 | Lymphedema (diagnosis) |
| 3 | Lymphedema (pathology) |
| 3 | Lymphoscintigraphy |
| 3 | Microcephaly (genetics) |
| 2 | Acute myelogenous leukemia |
| 2 | Amino Acid Sequence |
| 2 | Animals |
| 2 | Base Sequence |
| 2 | Calcium-Binding Proteins (genetics) |
| 2 | Cohort Studies |
| 2 | Craniofacial Abnormalities (genetics) |
| 2 | Distichiasis |
| 2 | Family |
| 2 | Family Health |
| 2 | Genetic Predisposition to Disease |
| 2 | Genetic Predisposition to Disease (genetics) |
| 2 | Genotype |
| 2 | Human |
| 2 | Hydrops Fetalis (genetics) |
| 2 | Leukemia, Myeloid, Acute (genetics) |
| 2 | Lymphangiectasis, Intestinal (genetics) |
| 2 | Middle Aged |
| 2 | Retinal Diseases (genetics) |
| 2 | Retinal Dysplasia (genetics) |
| 2 | Sequence Analysis, DNA |
| 2 | Syndrome |
| 2 | Tumor Suppressor Proteins (genetics) |
| 2 | Vascular Endothelial Growth Factor Receptor-3 (genetics) |
| 2 | Young Adult |
| 1 | Abnormalities, Multiple |
| 1 | Abnormalities, Multiple (genetics) |
| 1 | Alleles |
| 1 | Anemia, Hemolytic, Congenital (genetics) |
| 1 | Aortic Coarctation (diagnosis) |
| 1 | Aortic Coarctation (pathology) |
| 1 | Aortic coarctation |
| 1 | Autosomal character |
| 1 | Blotting, Western |
| 1 | Case study |
| 1 | Cholestasis (genetics) |
| 1 | Chorioretinopathy |
| 1 | Chromosome Deletion |
| 1 | Chromosome Mapping |
| 1 | Chromosomes, Human, Pair 11 |
| 1 | Chromosomes, Human, Pair 15 (genetics) |
| 1 | Chromosomes, Human, Pair 18 (genetics) |
| 1 | Chromosomes, Human, Pair 5 (genetics) |
| 1 | Chromosomes, Human, Pair 7 |
| 1 | Congenital |
| 1 | Congenital Abnormalities (genetics) |
| 1 | Congenital cardiopathy |
| 1 | Connexins (genetics) |
| 1 | Craniofacial Abnormalities (diagnosis) |
| 1 | Craniofacial Abnormalities (diagnostic imaging) |
| 1 | DNA |
| 1 | DNA Copy Number Variations |
| 1 | DNA Mutational Analysis (methods) |
| 1 | DNA-Binding Proteins (genetics) |
| 1 | Databases, Genetic |
| 1 | De novo |
| 1 | Diagnosis, Differential |
| 1 | Dominant character |
| 1 | Ectodermal Dysplasia (diagnosis) |
| 1 | Edema (diagnosis) |
| 1 | Edema (genetics) |
| 1 | Electroretinography |
| 1 | Exome |
| 1 | Failure to Thrive (diagnosis) |
| 1 | Fatal Outcome |
| 1 | Fetal Death |
| 1 | Fetus |
| 1 | Forkhead Transcription Factors |
| 1 | Forkhead Transcription Factors (genetics) |
| 1 | Frameshift Mutation (genetics) |
| 1 | GATA2 Transcription Factor (genetics) |
| 1 | GATA2 Transcription Factor (metabolism) |
| 1 | Gene Expression Regulation, Neoplastic |
| 1 | Gene Frequency |
| 1 | Genes, Recessive |
| 1 | Genetic Association Studies |
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