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You searched for: Author/Creator Sikkema-Raddatz, Birgit Subject 616.042

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1. Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome. Issue 3 (12th January 2013)

2. TBX4 mutations (small patella syndrome) are associated with childhood-onset pulmonary arterial hypertension. Issue 8 (16th April 2013)

3. Under-reported aspects of diagnosis and treatment addressed in the Dutch-Flemish guideline for comprehensive diagnostics in disorders/differences of sex development. Issue 9 (17th April 2020)

4. Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephaly. Issue 1 (December 2015)