List of bibliographic references
Number of relevant bibliographic references: 5.
List of associated KwdEn.i
Nombre de
documents | Descripteur |
|---|
| 4 | Humans |
| 3 | Beckwith-Wiedemann Syndrome (diagnosis) |
| 3 | Beckwith-Wiedemann Syndrome (genetics) |
| 2 | Chromosomes, Human, Pair 11 (genetics) |
| 2 | Female |
| 2 | Genetic Testing (standards) |
| 2 | Male |
| 2 | Silver-Russell Syndrome (diagnosis) |
| 2 | Silver-Russell Syndrome (genetics) |
| 1 | Alleles |
| 1 | Angelman Syndrome (genetics) |
| 1 | Child |
| 1 | Child, Preschool |
| 1 | Chromosome Aberrations |
| 1 | Chromosomes, Human (genetics) |
| 1 | Chromosomes, Human, Pair 15 (genetics) |
| 1 | Cohort Studies |
| 1 | CpG Islands (genetics) |
| 1 | Cyclin-Dependent Kinase Inhibitor p57 (genetics) |
| 1 | DNA Methylation (genetics) |
| 1 | Epigenesis, Genetic (genetics) |
| 1 | Europe |
| 1 | Genetic Counseling (methods) |
| 1 | Genetic Counseling (standards) |
| 1 | Genetic Testing |
| 1 | Genetic Testing (methods) |
| 1 | Genome, Human (genetics) |
| 1 | Genomic Imprinting |
| 1 | Genomic Imprinting (genetics) |
| 1 | Hypoplasia |
| 1 | Infant |
| 1 | Infant, Newborn |
| 1 | Insulin-Like Growth Factor II (genetics) |
| 1 | Intellectual Disability (genetics) |
| 1 | KCNQ1 Potassium Channel (genetics) |
| 1 | Karyotype |
| 1 | Microtubule-Associated Proteins (genetics) |
| 1 | Mutation |
| 1 | Nervous system diseases |
| 1 | Parents |
| 1 | Practice Guidelines as Topic |
| 1 | Prader-Willi Syndrome (genetics) |
| 1 | Prenatal Diagnosis (methods) |
| 1 | Prenatal Diagnosis (standards) |
| 1 | RNA, Long Noncoding (genetics) |
| 1 | Reproducibility of Results |
| 1 | Sequence Analysis, RNA |
| 1 | Societies, Medical |
| 1 | Uniparental Disomy (genetics) |
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