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The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
Despite the clinical significance of balanced chromosomal abnormalities (BCAs), their characterization has largely been restricted to cytogenetic resolution. We explored the landscape of BCAs at… Expand
Auditory Skills Development among Children with Developmental Delays and Cochlear Implants
- S. Wiley, J. Meinzen-Derr, D. Choo
- The Annals of otology, rhinology, and laryngology
- 1 October 2008
Objectives: We sought to understand auditory skills outcomes in young children with cochlear implants and developmental delay. Methods: Children who received cochlear implants at less than 36 months… Expand
Perceived qualitative benefits of cochlear implants in children with multi-handicaps.
- S. Wiley, Margaret L Jahnke, J. Meinzen-Derr, D. Choo
- International journal of pediatric…
- 1 June 2005
OBJECTIVE To determine families' perceived benefits of cochlear implants in children with multiple-handicaps. METHODS Parents/guardians of a child with a cochlear implant for at least 3 months,… Expand
Children with cochlear implants and developmental disabilities: a language skills study with developmentally matched hearing peers.
- J. Meinzen-Derr, S. Wiley, Sandra M Grether, D. Choo
- Psychology, Medicine
- Research in developmental disabilities
- 1 March 2011
The number of children receiving cochlear implants (CIs) with significant disabilities in addition to their deafness has increased substantially. Unfortunately, children with additional disabilities… Expand
Language performance in children with cochlear implants and additional disabilities
Quantify post‐cochlear implant (CI) language among children with disabilities and determine the role of nonverbal cognitive quotients (NVCQ) in predicting language.
Rubinstein‐Taybi syndrome medical guidelines
- S. Wiley, Susan Swayne, J. Rubinstein, N. Lanphear, C. Stevens
- American journal of medical genetics. Part A
- 1 June 2003
Children and adults with Rubinstein‐Taybi Syndrome have specific medical conditions that occur with greater frequency than the general population. Based on the available information from the… Expand
Update: Interim Guidance for the Diagnosis, Evaluation, and Management of Infants with Possible Congenital Zika Virus Infection — United States, October 2017
- Tolulope Adebanjo, Shana Godfred-Cato, +81 authors C. Zahn
- MMWR. Morbidity and mortality weekly report
- 20 October 2017
CDC has updated its interim guidance for U.S. health care providers caring for infants with possible congenital Zika virus infection (1) in response to recently published updated guidance for health… Expand
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations
- N. Mahdieh, B. Rabbani, S. Wiley, M. Akbari, S. Zeinali
- Biology, Medicine
- Journal of Human Genetics
- 1 October 2010
Hearing loss (HL) is the most prevalent sensory defect affecting 1 in 500 neonates. Genetic factors are involved in half of the cases. The extreme heterogeneity of HL makes it difficult to analyze… Expand
Autism spectrum disorders in 24 children who are deaf or hard of hearing.
- J. Meinzen-Derr, S. Wiley, S. Bishop, P. Manning-Courtney, D. Choo, D. Murray
- International journal of pediatric…
OBJECTIVES Approximately 4% of children who are deaf or hard of hearing have co-occurring autism spectrum disorder (ASD). Making an additional diagnosis of ASD in this population can be challenging,… Expand
Needs of parents of children who are deaf/hard of hearing with autism spectrum disorder.
- S. Wiley, Samantha J Gustafson, Justin Rozniak
- Medicine, Psychology
- Journal of deaf studies and deaf education
Little is known about children who are deaf or hard of hearing (D/HH) with a coexisting autism spectrum disorder (ASD). The objective of our study was to understand the needs of children who are D/HH… Expand