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American Journal of Medical Genetics|November 1, 1986
New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement--the CFC syndromeJ F Reynolds, G Neri, J P Herrmann, et al.American Journal of Medical Genetics. Supplement|January 1, 1987
The Montana Fetal Genetic Pathology Program and a review of prenatal death in humansJ M Opitz, J M FitzGerald, J F Reynolds, et al.Birth Defects Original Article Series|January 1, 1977
Grebe chondrodysplasia and similar forms of severe short-limbed dwarfismG Romeo, J Zonana, R S Lachman, et al.British Journal of Cancer|November 1, 1987
DNA analysis of breast tumour fine needle aspirates using flow cytometryP A Levack, P Mullen, T J Anderson, et al.American Journal of Medical Genetics|July 16, 1999
Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?A Bohring, M Silengo, M Lerone, et al.American Journal of Medical Genetics|January 1, 1991
A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six casesM K Bofinger, J M Opitz, S W Soukup, et al.National Cancer Institute Monograph|December 1, 1984
Carcinogenic effects of monofunctional and bifunctional furocoumarinsM P Mullen, M A Pathak, J D West, et al.Journal of Behavioral Medicine|March 4, 2017
A smartphone "app"-delivered randomized factorial trial targeting physical activity in adultsJason Fanning, Sarah Roberts, Charles H Hillman, et al.Genetics|October 12, 2012
Genetic interactions between UNC-17/VAChT and a novel transmembrane protein in Caenorhabditis elegansEleanor A Mathews, Gregory P Mullen, Jonathan Hodgkin, et al.Pediatric Transplantation|May 24, 2012
Bilateral lung transplant for hereditary hemorrhagic telangiectasia in a pediatric patientMeghna V Misra, Mary P Mullen, Sara O Vargas, et al.Pageof 59