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Celia Delozier

TitleAssociate Clinical Professor
InstitutionUniversity of California San Francisco
DepartmentDean's Office
Address3333 California Street
San Francisco CA 94118
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. Zhu VW, Hinduja S, Knezevich SR, Silveira WR, DeLozier CD. A rare case of choroid plexus carcinoma that led to the diagnosis of Lynch syndrome (hereditary nonpolyposis colorectal cancer). Clin Neurol Neurosurg. 2017 Jul; 158:46-48. PMID: 28460341.
      View in: PubMed
    2. Reinstein E, DeLozier CD, Simon Z, Bannykh S, Rimoin DL, Curry CJ. Ehlers-Danlos syndrome type VIII is clinically heterogeneous disorder associated primarily with periodontal disease, and variable connective tissue features. Eur J Hum Genet. 2013 Feb; 21(2):233-6. PMID: 22739343; PMCID: PMC3548259.
    3. Curry CJ, Bhullar S, Holmes J, Delozier CD, Roeder ER, Hutchison HT. Risk factors for perinatal arterial stroke: a study of 60 mother-child pairs. Pediatr Neurol. 2007 Aug; 37(2):99-107. PMID: 17675024.
      View in: PubMed
    4. Bugge M, Collins A, Hertz JM, Eiberg H, Lundsteen C, Brandt CA, Bak M, Hansen C, Delozier CD, Lespinasse J, Tranebjaerg L, Hahnemann JM, Rasmussen K, Bruun-Petersen G, Duprez L, Tommerup N, Petersen MB. Non-disjunction of chromosome 13. Hum Mol Genet. 2007 Aug 15; 16(16):2004-10. PMID: 17584770.
      View in: PubMed
    5. Thomas AC, Cullup T, Norgett EE, Hill T, Barton S, Dale BA, Sprecher E, Sheridan E, Taylor AE, Wilroy RS, DeLozier C, Burrows N, Goodyear H, Fleckman P, Stephens KG, Mehta L, Watson RM, Graham R, Wolf R, Slavotinek A, Martin M, Bourn D, Mein CA, O'Toole EA, Kelsell DP. ABCA12 is the major harlequin ichthyosis gene. J Invest Dermatol. 2006 Nov; 126(11):2408-13. PMID: 16902423.
      View in: PubMed
    6. Soravia C, DeLozier CD, Dobbie Z, Berthod CR, Arrigoni E, Br√ľndler MA, Blouin JL, Foulkes WD, Hutter P. Double frameshift mutations in APC and MSH2 in the same individual. Int J Colorectal Dis. 2006 Jan; 21(1):79-83. PMID: 16676398.
      View in: PubMed
    7. Soravia C, DeLozier CD, Dobbie Z, Berthod CR, Arrigoni E, Br√ľndler MA, Blouin JL, Foulkes WD, Hutter P. Double frameshift mutations in APC and MSH2 in the same individual. Int J Colorectal Dis. 2005 Sep; 20(5):466-470. PMID: 15834612.
      View in: PubMed