Skip to main content
U.S. flag

An official website of the United States government

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Search help
25 results
  1. Loeys-Dietz Syndrome - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1133
    ... Variants Database - TGFB3 TGFB3 database TGFB3 TGFB3 TGFBR1 9q22 ​.33 TGF-beta receptor type-1 TGFBR1 database ... Carter NP, Cormier-Daire V, Colleaux L. Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a ...
  2. Developmental Disabilities 
    https://medlineplus.gov/developmentaldisabilities.html
    Developmental disabilities can be physical, mental, or both. The problems are usually life-long, but therapy can help. Learn more. ... What are developmental ...
  3. Adult Central Nervous System Tumors Treatment (PDQ®) - PDQ Cancer Information Summaries - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK65982
    ... type 2 (5q21). Nevoid basal cell carcinoma syndrome (9q22.3). Clinical Features The clinical presentation of various ...
  4. Skin Cancer 
    https://medlineplus.gov/skincancer.html
    Try ABCDE on a mole to check for signs of skin cancer: Asymmetry, Border, Color, Diameter, Elevation. Learn more on advanced detection and treatments. ...
  5. Xeroderma Pigmentosum - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1397
    ... DNA polymerase eta POLH database POLH POLH XPA 9q22 ​.33 DNA repair protein complementing XP-A cells ...
  6. Nail-Patella Syndrome - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1132
    ... Kalscheuer V, Michalova K, Tommerup N. Interstitial deletion 9q22.32-q33.2 associated with additional familial translocation ...
  7. SPTLC1-Related Hereditary Sensory Neuropathy - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1390
    ... Locus Protein Locus-Specific Databases HGMD ClinVar SPTLC1 9q22 ​.31 Serine palmitoyltransferase 1 SPTLC1 @ LOVD SPTLC1 SPTLC1 ...
  8. ROR2-Related Robinow Syndrome - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1240
    ... Locus Protein Locus-Specific Databases HGMD ClinVar ROR2 9q22 ​.31 Tyrosine-protein kinase transmembrane receptor ROR2 ROR2 @ ...
  9. Fanconi Anemia - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1401
    ... Fanconi Anaemia Mutation Database (FANCB) FANCB FANCB FANCC 9q22 ​.32 Fanconi anemia group C protein Fanconi Anemia ...
  10. 9q22.3 microdeletion 
    https://medlineplus.gov/genetics/condition/9q223-microdeletion
    9q22.3 microdeletion is a chromosomal change in which a small piece of chromosome 9 is deleted ... condition called Gorlin syndrome.Many individuals with a 9q22.3 microdeletion have delayed development, particularly affecting the ...
previous · 1 · 2 · 3 · next