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13. Okur‐Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansion. Issue 4 (13th February 2018)

17. TBL1XR1 mutations in Pierpont syndrome are not restricted to the recurrent p.Tyr446Cys mutation. Issue 12 (26th October 2018)

18. Wiedemann‐Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases. Issue 1 (17th May 2018)

19. 努南综合征的皮肤病表现. (1st June 2019)

20. 努南综合征的皮肤病表现. (3rd June 2019)