Group by:
Item Type |
DateNumber of items: 1.
Journal article
Umair, M.; Eckstein, G.; Rudolph, G.; Strom, T.; Graf, E.; Hendig, D.; Hoover, J.; Alanay, J.; Meitinger, T.; Schmidt, H. und Ahmad, W.
(2018):
Homozygous XYLT2 variants as a cause of spondyloocular syndrome.
In: Clinical Genetics, Vol. 93, No. 4: pp. 913-918
This list was generated on Sun Dec 8 02:48:18 2024 CET.