VIICTR
Profiles
ORIT
Pediatrics CRA
Home
About
Overview
Sharing Data
ORCID
Help
History (0)
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Search Result Details
Back to Search Results
This page shows the details of why an item matched the keywords from your search.
Search Results
BALLABIO, ANDREA
One or more keywords matched the following items that are connected to
BALLABIO, ANDREA
Item Type
Name
Academic Article
Deletion spanning the 5' ends of both the COL4A5 and COL4A6 genes in a patient with Alport's syndrome and leiomyomatosis.
Academic Article
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation.
Academic Article
LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosis.
Academic Article
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome.
Academic Article
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene.
Academic Article
Molecular diagnosis of Alport syndrome: the experience in Siena.
Academic Article
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?
Academic Article
Evidence for genetic heterogeneity in benign familial hematuria.
Concept
Nephritis, Hereditary
Search Criteria
Nephritis Hereditary