European journal of human genetics : EJHG, 2010-01, Vol.18 (1), p.8-14
2010
Details
- Autor(en) / Beteiligte
- Titel
- Beckwith-Wiedemann syndrome
- Ist Teil von
- European journal of human genetics : EJHG, 2010-01, Vol.18 (1), p.8-14
- Ort / Verlag
- Basingstoke: Nature Publishing Group
- Erscheinungsjahr
- 2010
- Link zum Volltext
- Quelle
- MEDLINE
- Beschreibungen/Notizen
- Beckwith-Wiedemann syndrome (BWS) is a model disorder for the study of imprinting, growth dysregulation, and tumorigenesis. Unique observations in this disorder point to an important embryonic developmental window relevant to the observations of increased monozygotic twinning and an increased rate of epigenetic errors after subfertility/assisted reproduction.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 1018-4813eISSN: 1476-5438DOI: 10.1038/ejhg.2009.106Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2987155
- Format
- –
- Schlagworte
- Abdomen, Beckwith-Wiedemann Syndrome - diagnosis, Beckwith-Wiedemann Syndrome - genetics, Beckwith-Wiedemann Syndrome - therapy, Biological and medical sciences, Cardiomyopathy, Childbirth & labor, Chromosomes, Classical genetics, quantitative genetics, hybrids, Diagnosis, Differential, Epigenetics, Fundamental and applied biological sciences. Psychology, General aspects. Genetic counseling, Genetic Counseling, Genetic Testing, Genetics, Genetics of eukaryotes. Biological and molecular evolution, Hernias, Human, Humans, Hypoglycemia, Kidneys, Medical genetics, Medical sciences, Metabolism, Molecular and cellular biology, Pediatrics, Practical Genetics, Surveillance, Tumors