Facial phenotype allows diagnosis of Mowat-Wilson syndrome in the absence of Hirschsprung disease
Horn, Denise; Weschke, Bernhard; Zweier, Christiane; Rauch, Anita (2004). Facial phenotype allows diagnosis of Mowat-Wilson syndrome in the absence of Hirschsprung disease. American Journal of Medical Genetics. Part A, 124A(1):102-104.
Additional indexing
Item Type: | Journal Article, refereed, original work |
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Communities & Collections: | 04 Faculty of Medicine > Institute of Medical Genetics |
Dewey Decimal Classification: | 570 Life sciences; biology
610 Medicine & health |
Scopus Subject Areas: | Life Sciences > Genetics
Health Sciences > Genetics (clinical) |
Language: | English |
Date: | 1 January 2004 |
Deposited On: | 09 Jun 2021 08:49 |
Last Modified: | 24 Apr 2025 01:35 |
Publisher: | Wiley-Blackwell Publishing, Inc. |
ISSN: | 1552-4825 |
OA Status: | Closed |
Free access at: | Publisher DOI. An embargo period may apply. |
Publisher DOI: | https://doi.org/10.1002/ajmg.a.20298 |
PubMed ID: | 14679597 |
Permanent URL
https://doi.org/10.5167/uzh-203915Download
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