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2. Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS–FREM complex disorders. Issue 12 (24th September 2013)

3. Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS–FREM complex disorders. Issue 12 (24th September 2013)

6. Cantú syndrome: Findings from 74 patients in the International Cantú Syndrome Registry. Issue 4 (11th December 2019)

7. Cover Image, Volume 176A, Number 5, May 2018. Issue 5 (21st April 2018)

8. De novo 14q24.2q24.3 microdeletion including IFT43 is associated with intellectual disability, skeletal anomalies, cardiac anomalies, and myopia. Issue 6 (19th February 2016)

9. De Novo Trisomy 1q10q23.3 Mosaicism Causes Microcephaly, Severe Developmental Delay, and Facial Dysmorphic Features but No Cardiac Anomalies. (31st January 2016)