SandraLouise HyvarinenDavenportMD

PubMed

• 2 citations
  An intragenic deletion of the gene MNAT1 in a family with pectus deformities
  Jennifer L. Heithaus, Sandra Davenport, Kimberly A. Twyman, Erin Torti, Jacqueline R. Batanian> ;American Journal of Medical Genetics. Part A. 2014 May 1
• 19 citations
  Understanding obstructive sleep apnea in children with CHARGE syndrome
  Carrie-Lee Trider, Gerard Corsten, Debra Morrison, Margaret A. Hefner, Sandra Davenport, Kim Blake> ;International Journal of Pediatric Otorhinolaryngology. 2012 Jul 1
• 20 citations
  Toward a genetic etiology of CHARGE syndrome: I. A systematic scan for submicroscopic deletions.
  Seema R. Lalani, David W. Stockton, Carlos A. Bacino, Laura Molinari, Nancy L. Glass, Susan D. Fernbach, Jeffrey A. Towbin, William J. Craigen, John M. Graham, Margare...> ;American Journal of Medical Genetics. Part A. 2003 Apr 30
• 48 citations
  Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion.
  James A. Bartley, Shivanand Patil, Sandra L.H. Davenport, David E. Goldstein, James M. Pickens> ;The Journal of Pediatrics. 1986 Feb 1
• 3 citations
  A medical microcomputer database management system.
  Joyce A. Mitchell, A. R. Naddaf-Dezfoli, Sandra L.H. Davenport> ;Methods of Information in Medicine. 1985 Apr 1
• 25 citations
  Usher syndrome in four hard-of-hearing siblings.
  Sandra L. H. Davenport, Sinead O'Nuallain, Gilbert S. Omenn, Robert J. Wilkus> ;Pediatrics. 1978 Oct 1
• 2 citations
  Juvenile diabeties mellitus, optic atrophy, sensory nerve deafness, and diabetes insipidus—a syndrome
  Sandra L.H. Davenport> ;The Journal of Pediatrics. 1977 May 1
• Genetic studies of Usher syndrome.
  Kimberling, W. J., Weston, M. D., Pieke Dahl, S., Kenyon, J. B., Shugart, Y. Y., Moller, C., Davenport, S. L., Martini, A., Milani, M., Smith, R. J.> ;Ann N Y Acad Sci. 1991
• Localization of Usher syndrome type II to chromosome 1q.
  Kimberling, W. J., Weston, M. D., Möller, C., Davenport, S. L., Shugart, Y. Y., Priluck, I. A., Martini, A., Milani, M., Smith, R. J.> ;Genomics. 1990 Jun
• The child with multiple congenital anomalies.
  Davenport, S. L.> ;Pediatr Ann. 1990 Jan
• Dominant hearing loss, white hair, contractures, hyperkeratotic papillomata, and depressed chemotaxis.
  Davenport, S. L., Donlan, M. A., Dolan, C. R., Ochs, H. D.> ;Birth Defects Orig Artic Ser. 1979
• Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11.
  Kimberling, W. J., Möller, C. G., Davenport, S., Priluck, I. A., Beighton, P. H., Greenberg, J., Reardon, W., Weston, M. D., Kenyon, J. B., Grunkemeyer, J. A.> ;Genomics. 1992 Dec
• Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
  Eudy, J. D., Weston, M. D., Yao, S., Hoover, D. M., Rehm, H. L., Ma-Edmonds, M., Yan, D., Ahmad, I., Cheng, J. J., Ayuso, C., Cremers, C., Davenport, S., Moller, C., T...> ;Science. 1998 Jun 12
• Usher syndrome: an otoneurologic study.
  Möller, C. G., Kimberling, W. J., Davenport, S. L., Priluck, I., White, V., Biscone-Halterman, K., Odkvist, L. M., Brookhouser, P. E., Lund, G., Grissom, T. J.> ;Laryngoscope. 1989 Jan
• Cowden disease: gene marker studies and measurements of epidermal growth factor.
  Carlson, H. E., Burns, T. W., Davenport, S. L., Luger, A. M., Spence, M. A., Sparkes, R. S., Orth, D. N.> ;Am J Hum Genet. 1986 Jun
• 60 citations
  Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes.
  Roberta A. Pagon, Judith G. Hall, Sandra L.H. Davenport, J Aase, T H Norwood, Holger Hoehn> ;American Journal of Human Genetics. 1979 Jan 1
• Usher syndrome: clinical findings and gene localization studies.
  Kimberling, W. J., Möller, C. G., Davenport, S. L., Lund, G., Grissom, T. J., Priluck, I., White, V., Weston, M. D., Biscone-Halterman, K., Brookhouser, P. E.> ;Laryngoscope. 1989 Jan
• Early experience with the gamma interlocking nail for peritrochanteric fractures of the proximal femur.
  Lindsey, R. W., Teal, P., Probe, R. A., Rhoads, D., Davenport, S., Schauder, K.> ;J Trauma. 1991 Dec
• 3 citations
  A new expert consultation system in deaf-blind syndromes
  Joyce A. Mitchell, Sandra L.H. Davenport, Margaret A. Hefner, Monli Molly Shei> ;Medical Informatics = Medecine Et Informatique. 1986 Jan 1
• Multiple congenital anomalies. An approach to management.
  Davenport, S. L.> ;Pediatrician. 1988
• 20 citations
  Use of an expert model to test diagnostic criteria in CHARGE syndrome
  Joyce A. Mitchell, Sandra L.H. Davenport, Margaret A. Hefner, Monli Molly Shei> ;Journal of Medical Systems. 1985 Dec 1
• Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes.
  Annunen, S., Körkkö, J., Czarny, M., Warman, M. L., Brunner, H. G., Kääriäinen, H., Mulliken, J. B., Tranebjaerg, L., Brooks, D. G., Cox, G. F., Cruysberg, J. R., Curt...> ;Am J Hum Genet. 1999 Oct
• 319 citations
  CHARGE Association: An Update and Review for the Primary Pediatrician
  Kim Blake, Sandra L.H. Davenport, Bryan D. Hall, Margaret A. Hefner, Roberta A Pagon, Marc S. Williams, Angela E. Lin, John M. Graham> ;Clinical Pediatrics. 1998 Mar 1
• 102 citations
  The spectrum of clinical features in CHARGE syndrome
  Sandra L.H. Davenport, Margaret A. Hefner, Joyce A. Mitchell> ;Clinical Genetics. 2008 Apr 23
• 32 citations
  CHARGE syndrome. Part II. Hearing loss.
  James W. Thelin, Joyce A. Mitchell, Margaret A. Hefner, Sandra L.H. Davenport> ;International Journal of Pediatric Otorhinolaryngology. 1986 Dec 1
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