Parents

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Robert Cooley Elderfield grad student 1942 Columbia
 (Alstonia alkaloids. I. Degradation of alstonine to [beta]-carboline bases and the reduction of tetrahydroalstonine with sodium and butyl alcohol.)
Roger Adams post-doc UIUC

Children

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Marc d'Alarcao grad student UIUC
Alexander Jerry Kresge grad student 1953 UIUC
Allan S. Hay grad student 1955 UIUC
W. Kenneth Musker grad student 1959 UIUC
James Alden Deyrup grad student 1961 UIUC
Carl Randolph Johnson grad student 1962 UIUC
Richard A. Laursen grad student 1964 UIUC
Douglas T. Browne grad student 1964-1968 UIUC
Sidney M. Hecht grad student 1970 UIUC
Graham C. Walker grad student 1974 UIUC
David F. Wiemer grad student 1976 UIUC
Anthony W. Czarnik grad student 1981 UIUC
Alan M Jones grad student 1978-1983 (Plant Biology Tree)
Dee Ann Casteel grad student 1979-1985 UIUC
John P Helgeson post-doc 1964-1966 UIUC (Computational Biology Tree)
Vasu Nair post-doc 1966-1968 UIUC
Donald Eugene Bergstrom post-doc 1970-1972 UIUC
Ulrich Jordis post-doc 1983-1983 UIUC
BETA: Related publications

Publications

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Gripp KW, Hopkins E, Serrano A, et al. (2012) Transmission of the rare HRAS mutation (c. 173C > T; p.T58I) further illustrates its attenuated phenotype. American Journal of Medical Genetics. Part A. 158: 1095-101
Joynt CA, Robertson CM, Cheung PY, et al. (2009) Two-year neurodevelopmental outcomes of infants undergoing neonatal cardiac surgery for interrupted aortic arch: a descriptive analysis. The Journal of Thoracic and Cardiovascular Surgery. 138: 924-32
Gripp KW, Innes AM, Axelrad ME, et al. (2008) Costello syndrome associated with novel germline HRAS mutations: an attenuated phenotype? American Journal of Medical Genetics. Part A. 146: 683-90
Kolski HK, Leonard NJ, Lemmers RJ, et al. (2008) Atypical facet of Möbius syndrome: association with facioscapulohumeral muscular dystrophy. Muscle & Nerve. 37: 526-9
Bhargava R, Leonard NJ, Chan AK, et al. (2005) Autosomal dominant inheritance of spondyloenchondrodysplasia. American Journal of Medical Genetics. Part A. 135: 282-8
Leonard NJ, Krol AL, Bleoo S, et al. (2005) Sensorineural hearing loss, striate palmoplantar hyperkeratosis, and knuckle pads in a patient with a novel connexin 26 (GJB2) mutation. Journal of Medical Genetics. 42: e2
Leonard NJ. (2002) A second patient with MCA/MR syndrome with multiple circumferential skin creases. American Journal of Medical Genetics. 112: 91-4
Leonard NJ, Tomkins DJ. (2002) Diploid/tetraploid/t(1;6) mosaicism in a 17-year-old female with hypomelanosis of Ito, multiple congenital anomalies, and body asymmetry. American Journal of Medical Genetics. 112: 86-90
Sazgar M, Leonard NJ, Renaud DL, et al. (2002) Intracranial calcification, retinopathy, and osteopenia: a new syndrome? Pediatric Neurology. 26: 324-8
Christian SM, Kieffer SA, Leonard NJ. (2001) Medical genetics and patient use of the Internet. Clinical Genetics. 60: 232-6
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