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Craniofrontonasal syndrome in a male due to chromosomal mosaicism involving EFNB1: further insights into a genetic paradox
Evers, C., Jungwirth, M.S., Morgenthaler, J., Hinderhofer, K., Maas, B., Janssen, J.W.G., Jauch, A., Hehr, U., Steinbeisser, H. and Moog, U. (2014) Craniofrontonasal syndrome in a male due to chromosomal mosaicism involving EFNB1: further insights into a genetic paradox. Clinical Genetics 85 (4), pp. 347-353.Date of publication of this fulltext: 19 Dec 2024 08:12
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| Item type | Article | ||||
| Journal or Publication Title | Clinical Genetics | ||||
| Publisher: | WILEY-BLACKWELL | ||||
|---|---|---|---|---|---|
| Place of Publication: | HOBOKEN | ||||
| Volume: | 85 | ||||
| Number of Issue or Book Chapter: | 4 | ||||
| Page Range: | pp. 347-353 | ||||
| Date | 2014 | ||||
| Institutions | Medicine > Lehrstuhl für Humangenetik | ||||
| Identification Number |
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| Keywords | MUTATIONS; EPHRIN-B1; EPH; HYBRIDIZATION; REVERSE; craniofrontonasal syndrome; EFNB1; ephrin-B1; mosaicism; supernumerary ring X chromosome | ||||
| Dewey Decimal Classification | 600 Technology > 610 Medical sciences Medicine | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Yes | ||||
| Item ID | 61627 |
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