Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.

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  1. Milunsky JM, Maher TM, Zhao G, Wang Z, Mulliken JB, Chitayat D, Clemens M, Stalker HJ, Bauer M, Burch M, Chénier S, Cunningham ML, Drack AV, Janssens S, Karlea A, Klatt R, Kini U, Klein O, Lachmeijer AM, Megarbane A, Mendelsohn NJ, Meschino WS, Mortier GR, Parkash S, Ray CR, Roberts A, Roberts A, Reardon W, Schnur RE, Smith R, Splitt M, Tezcan K, Whiteford ML, Wong DA, Zori R, Lin AE. Genotype-phenotype analysis of the branchio-oculo-facial syndrome. Am J Med Genet A. 2011 Jan; 155A(1):22-32.View Related Profiles. PMID: 21204207; DOI: 10.1002/ajmg.a.33783;
  2. Leon E, Zou YS, Milunsky JM. Mosaic Down syndrome in a patient with low-level mosaicism detected by microarray. Am J Med Genet A. 2010 Dec; 152A(12):3154-6.View Related Profiles. PMID: 21108401; DOI: 10.1002/ajmg.a.33739;
  3. Jamal SM, Basran RK, Newton S, Wang Z, Milunsky JM. Novel de novo PCDH19 mutations in three unrelated females with epilepsy female restricted mental retardation syndrome. Am J Med Genet A. 2010 Oct; 152A(10):2475-81.View Related Profiles. PMID: 20830798; DOI: 10.1002/ajmg.a.33611;
  4. Milunsky A, Ito M, Maher TA, Flynn M, Milunsky JM. Prenatal molecular diagnosis of tuberous sclerosis complex. Am J Obstet Gynecol. 2009 Mar; 200(3):321.e1-6.View Related Profiles. PMID: 19254590; DOI: 10.1016/j.ajog.2008.11.004;

This graph shows the total number of publications by year, by first, middle/unknown, or last author.

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