Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

1995
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 1
1997 1
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Search Results

2 results

Results by year

Filters applied: . Clear all
Page 1
Neuroectodermal (CHIME) syndrome: an additional case with long term follow up of all reported cases.
Shashi V, Zunich J, Kelly TE, Fryburg JS. Shashi V, et al. J Med Genet. 1995 Jun;32(6):465-9. doi: 10.1136/jmg.32.6.465. J Med Genet. 1995. PMID: 7666399 Free PMC article. Review.
A new neuroectodermal syndrome (designated CHIME syndrome) was described in 1983 with a total of four patients reported, it is presumed to be an autosomal recessive disorder because of recurrence in sibs. ...
A new neuroectodermal syndrome (designated CHIME syndrome) was described in 1983 with a total of four patients reported, it is …
Acute lymphoblastic leukemia in a child with the CHIME neuroectodermal dysplasia syndrome.
Schnur RE, Greenbaum BH, Heymann WR, Christensen K, Buck AS, Reid CS. Schnur RE, et al. Am J Med Genet. 1997 Oct 3;72(1):24-9. Am J Med Genet. 1997. PMID: 9295069 Review.
The "CHIME" syndrome (MIM#280000) is a rare neuroectodermal disorder comprised of Colobomas of the eye, Heart defects, Ichthyosiform dermatosis, Mental retardation, and Ear defects. ...Histologic examination of the skin demonstrated findings of an epidermal nevus wi …
The "CHIME" syndrome (MIM#280000) is a rare neuroectodermal disorder comprised of Colobomas of the eye, Heart defects, Ichthyo …