S. Davenport

发表

Cowden disease: gene marker studies and measurements of epidermal growth factor.

M. Spence, D. Orth, R. Sparkes, 1986, American journal of human genetics.

Understanding obstructive sleep apnea in children with CHARGE syndrome.

D. Morrison, K. Blake, S. Davenport, 2012, International journal of pediatric otorhinolaryngology.

Usher syndrome: Clinical findings and gene localization studies

C. Möller, W. Kimberling, M. D. Weston, 1989, The Laryngoscope.

Postoperative airway events of individuals with CHARGE syndrome.

M. Roy, T. Hartshorne, K. Blake, 2009, International journal of pediatric otorhinolaryngology.

Behavior in CHARGE syndrome: Introduction to the special topic

T. Hartshorne, S. Davenport, M. Hefner, 2005, American journal of medical genetics. Part A.

Toward a genetic etiology of CHARGE syndrome: I. A systematic scan for submicroscopic deletions

J. Belmont, J. Towbin, S. Lalani, 2003, American journal of medical genetics. Part A.

An intragenic deletion of the gene MNAT1 in a family with pectus deformities

J. Batanian, K. Twyman, E. Torti, 2014, American journal of medical genetics. Part A.

Usher syndrome: An otoneurologic study

C. Möller, W. Kimberling, P. Brookhouser, 1989, The Laryngoscope.

Psychological adjustment of adolescents with myelodysplasia

P. Hayden, S. Davenport, M. Campbell, 1977, Journal of youth and adolescence.

Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion.

S. Patil, J. Bartley, S. Davenport, 1986, The Journal of pediatrics.

Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes.

R. Pagon, H. Hoehn, T. Norwood, 1979, American journal of human genetics.

Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

H. Rehm, C. Cremers, C. Möller, 1998, Science.

CHARGE Association: An Update and Review for the Primary Pediatrician

Marc S. Williams, J. Graham, R. Pagon, 1998, Clinical pediatrics.

Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.

Leif E. Peterson, L. D. White, R. Gibbs, 2006, American journal of human genetics.

Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder

P. Stankiewicz, Z. Xia, S. Cheung, 2009, neurogenetics.

The spectrum of clinical features in CHARGE syndrome

S. Davenport, M. Hefner, Joyce A. Mitchell, 1986, Clinical genetics.

CHARGE syndrome. Part I. External ear anomalies.

J. Thelin, S. Davenport, M. Hefner, 1986, International journal of pediatric otorhinolaryngology.

CHARGE syndrome. Part II. Hearing loss.

J. Thelin, J. Mitchell, S. Davenport, 1986, International journal of pediatric otorhinolaryngology.

Use of an expert model to test diagnostic criteria in CHARGE syndrome

Joyce A. Mitchell, Margaret A. Hefner, Monli Molly Shei, 1985, Journal of Medical Systems.

Localization of Usher syndrome type II to chromosome 1q.

C. Möller, Y. Shugart, W. Kimberling, 1990, Genomics.

Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes.

D J Prockop, I. Kaitila, A. Latos-Bieleńska, 1999, American journal of human genetics.

Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11.

W. Reardon, P. Beighton, C. Möller, 1992, Genomics.

Adolescents with myelodysplasia: impact of physical disability on emotional maturation.

P. Hayden, S. Davenport, M. Campbell, 1979, Pediatrics.

Genetic Studies of Usher Syndrome

Y. Shugart, W. Kimberling, M. D. Weston, 1991, Annals of the New York Academy of Sciences.

Human ring chromosomes: a report of five cases.

D. Picciano, S. Davenport, C. B. Jacobson, 1972, Annales de genetique.

The child with multiple congenital anomalies.

S. Davenport, 1990, Pediatric annals.

Juvenile diabetes mellitus, optic atrophy, sensory nerve deafness, and diabetes insipidus--a syndrome.

S. Davenport, 1977, The Journal of pediatrics.

Usher syndrome in four hard-of-hearing siblings.

G. Omenn, R. Wilkus, S. O'Nualláin, 1978, Pediatrics.

A new expert consultation system in deaf-blind syndromes.

J. Mitchell, J A Mitchell, S L Davenport, 1986, Medical informatics = Medecine et informatique.