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3. FRA18C: a new aphidicolin-inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakage. Issue 5 (2nd May 2007)

5. Identification of Novel Craniofacial Regulatory Domains Located far Upstream of SOX9 and Disrupted in Pierre Robin Sequence. Issue 8 (August 2014)

6. Identification of STAC3 variants in non‐Native American families with overlapping features of Carey–Fineman–Ziter syndrome and Moebius syndrome. Issue 10 (4th August 2017)

7. Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1, 133 families with developmental disorders. (October 2018)

8. Phenotypes and genotypes in individuals with SMC1A variants. Issue 8 (26th May 2017)

10. The clinical significance of small copy number variants in neurodevelopmental disorders. Issue 10 (8th August 2014)