Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1994 1
1995 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

2 results

Results by year

Filters applied: . Clear all
Page 1
Deletion of the short arm of chromosome 10 (10p13): report of a patient and review.
Shapira M, Borochowitz Z, Bar-El H, Dar H, Etzioni A, Lorber A. Shapira M, et al. Am J Med Genet. 1994 Aug 1;52(1):34-8. doi: 10.1002/ajmg.1320520107. Am J Med Genet. 1994. PMID: 7977458 Review.
Since the first description by Elliot et al. [1970, Am J Dis Child 119:72-73] of a probable partial deletion of chromosome 10p, 17 other cases have been reported. ...We report on an additional case of 10p deletion syndrome and review the literature....
Since the first description by Elliot et al. [1970, Am J Dis Child 119:72-73] of a probable partial deletion of chromosome 10p …
DiGeorge syndrome and partial monosomy 10p: case report and review.
Schuffenhauer S, Seidel H, Oechsler H, Belohradsky B, Bernsau U, Murken J, Meitinger T. Schuffenhauer S, et al. Ann Genet. 1995;38(3):162-7. Ann Genet. 1995. PMID: 8540688 Review.
DiGeorge syndrome (DGS) is predominantly caused by partial monosomy 22q11, but a subset of patients with DGS show deletions of 10p or other chromosomal abnormalities. ...The common DGS mutation-microdeletion 22q11-was excluded by FISH analysis, and the breakpoints o …
DiGeorge syndrome (DGS) is predominantly caused by partial monosomy 22q11, but a subset of patients with DGS show deletions of …