MaryJane Hall(Hall)WillisMD

Clinical Genetics, Pediatric Medical Genetics

Physician

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University of California (San Diego) Medical CenterResidency, Medical Genetics and Genomics, 2004 - 2007
University of California (San Diego) Medical CenterResidency, Pediatrics, 1999 - 2003
University of Colorado School of Medicine Anschutz Medical CampusClass of 1999

PubMed

48 citations
Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly
Kelly A. Bear, Benjamin D. Solomon, Sonir Roberto Rauber Antonini, Ivo J.P. Arnhold, Marcela M. França, Erica H. Gerkes, Dorothy K. Grange, Donald W. Hadley, Jarmo Jää...> ;Journal of Medical Genetics. 2014 Apr 17
46 citations
Expanded clinical and molecular spectrum of guanidinoacetate methyltransferase (GAMT) deficiency.
Shweta U. Dhar, Fernando Scaglia, Fang yuan Li, Laurie D. Smith, Bruce A. Barshop, Christine M. Eng, Richard H. Haas, Jill V. Hunter, Timothy Lotze, Bruno Maranda, M. ...> ;Molecular Genetics and Metabolism. 2009 Jan 1
40 citations
CPT2 gene mutations resulting in lethal neonatal or severe infantile carnitine palmitoyltransferase II deficiency.
Paul J. Isackson, Michael J. Bennett, Uta Lichter-Konecki, M. J.H. Willis, William L. Nyhan, V. Reid Sutton, Ingrid Tein, Georgirene D. Vladutiu> ;Molecular Genetics and Metabolism. 2008 Aug 1
18 citations
Natural history of prenatally diagnosed 46,X,isodicentric Y.
M. J.H. Willis, Lynne M. Bird, M. Dell'Aquilla, Marilyn C. Jones> ;Prenatal Diagnosis. 2006 Feb 1
14 citations
Expanding the phenotype of mosaic trisomy 20
M. J.H. Willis, Lynne M. Bird, Marie Dell'Aquilla, Marilyn C. Jones> ;American Journal of Medical Genetics. Part A. 2008 Feb 1
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