These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Search MEDLINE/PubMed
Title: The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X. Author: Sutherland GR, Baker E. Journal: Clin Genet; 1990 Mar; 37(3):167-72. PubMed ID: 2323087. Abstract: The common fragile site on the end of the long arm of the human X chromosome has been shown to be at a different location from the rare fragile site which produces the fragile X syndrome of intellectual handicap. The different locations can be clearly seen in chromosomes at about the 550 band level of resolution. This finding should help resolve difficulties in fragile X cytogenetics where expression of the common fragile site can lead to false positive diagnoses.[Abstract] [Full Text] [Related] [New Search]