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
2002 1
2017 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

2 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "T-cell immunodeficiency, congenital alopecia, and nail dystrophy"
Page 1
A lesson for unraveling complex aspects of novel immunodeficiencies from the human equivalent of the nude/SCID phenotype.
Pignata C. Pignata C. J Hematother Stem Cell Res. 2002 Apr;11(2):409-14. doi: 10.1089/152581602753658592. J Hematother Stem Cell Res. 2002. PMID: 11983112 Review.
Similar to the mouse, the human phenotype is characterized by a profound T cell ontogenetic defect associated with congenital alopecia and nail dystrophy. ...The opportunity to study immunological reconstitution in the absence of a functi …
Similar to the mouse, the human phenotype is characterized by a profound T cell ontogenetic defect associated with congenit …
FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis.
Radha Rama Devi A, Panday NN, Naushad SM. Radha Rama Devi A, et al. Gene. 2017 Sep 5;627:222-225. doi: 10.1016/j.gene.2017.06.033. Epub 2017 Jun 19. Gene. 2017. PMID: 28636882
Mutation in FOXN1 was reported to cause a rare disorder characterized by rudimentary thymus gland, T-cell immunodeficiency, congenital alopecia and nail dystrophy within an Italian community. ...Immunological study of the proband r …
Mutation in FOXN1 was reported to cause a rare disorder characterized by rudimentary thymus gland, T-cell immunodeficiency …