No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia:
Gespeichert in:
| Hauptverfasser: | , , , |
|---|---|
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Erlangen ; Nürnberg
Friedrich-Alexander-Universität Erlangen-Nürnberg
2021
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| Schlagworte: | |
| Online-Zugang: | Volltext Volltext |
| Beschreibung: | 1 Online-Ressource |
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| spelling | Körber, Laura Verfasser aut No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia Laura Körber, Holm Schneider, Nicole Fleischer, Sigrun Maier-Wohlfart Erlangen ; Nürnberg Friedrich-Alexander-Universität Erlangen-Nürnberg 2021 1 Online-Ressource txt rdacontent c rdamedia cr rdacarrier Human genetics. Pharmacology. Medicine. Medicine/Public Health, general. Pharmacology/Toxicology. Human Genetics. Schneider, Holm Verfasser aut Fleischer, Nicole Verfasser aut Maier-Wohlfart, Sigrun Verfasser aut Sonderdruck aus Orphanet Journal of Rare Diseases Vol. 16 (2021) 10.1186/s13023-021-01735-2 https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-176714 Resolving-System kostenfrei Volltext https://open.fau.de/handle/openfau/17671 Verlag kostenfrei Volltext 1\p aepkn 0,83093 20210412 DE-101 https://d-nb.info/provenance/plan#aepkn 2\p aepsg 0,99990 20210412 DE-101 https://d-nb.info/provenance/plan#aepsg 3\p npi 20210411 DE-101 https://d-nb.info/provenance/plan#npi |
| spellingShingle | Körber, Laura Schneider, Holm Fleischer, Nicole Maier-Wohlfart, Sigrun No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia Human genetics. Pharmacology. Medicine. |
| title | No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia |
| title_auth | No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia |
| title_exact_search | No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia |
| title_exact_search_txtP | No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia |
| title_full | No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia Laura Körber, Holm Schneider, Nicole Fleischer, Sigrun Maier-Wohlfart |
| title_fullStr | No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia Laura Körber, Holm Schneider, Nicole Fleischer, Sigrun Maier-Wohlfart |
| title_full_unstemmed | No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia Laura Körber, Holm Schneider, Nicole Fleischer, Sigrun Maier-Wohlfart |
| title_short | No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia |
| title_sort | no evidence for preferential x chromosome inactivation as the main cause of divergent phenotypes in sisters with x linked hypohidrotic ectodermal dysplasia |
| topic | Human genetics. Pharmacology. Medicine. |
| topic_facet | Human genetics. Pharmacology. Medicine. |
| url | https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-176714 https://open.fau.de/handle/openfau/17671 |
| work_keys_str_mv | AT korberlaura noevidenceforpreferentialxchromosomeinactivationasthemaincauseofdivergentphenotypesinsisterswithxlinkedhypohidroticectodermaldysplasia AT schneiderholm noevidenceforpreferentialxchromosomeinactivationasthemaincauseofdivergentphenotypesinsisterswithxlinkedhypohidroticectodermaldysplasia AT fleischernicole noevidenceforpreferentialxchromosomeinactivationasthemaincauseofdivergentphenotypesinsisterswithxlinkedhypohidroticectodermaldysplasia AT maierwohlfartsigrun noevidenceforpreferentialxchromosomeinactivationasthemaincauseofdivergentphenotypesinsisterswithxlinkedhypohidroticectodermaldysplasia |