Search

Search Constraints

You searched for: Author/Creator Fox, Deborah J.

Search Results

1. Association of genetic mutations and loss of ambulation in childhood‐onset dystrophinopathy. Issue 2 (17th November 2020)

2. Cardiovascular health supervision for Duchenne Muscular Dystrophy; data from the MD STARnet. (March 2018)

6. Methods for surveillance of fetal alcohol syndrome: The fetal alcohol syndrome surveillance network II (FASSNetII) – Arizona, Colorado, New York, 2009 ‐ 2014. Issue 3 (12th March 2015)

7. Muscular Dystrophy Surveillance, Tracking, and Research Network pilot: Population‐based surveillance of major muscular dystrophies at four U.S. sites, 2007–2011. Issue 19 (2nd August 2018)

8. Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis. Issue 3 (March 2016)

9. Population‐based microcephaly surveillance in the United States, 2009 to 2013: An analysis of potential sources of variation. Issue 11 (November 2016)

10. Reproductive patterns among mothers of males diagnosed with Duchenne or Becker muscular dystrophy123. Issue 1 (13th December 2012)