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 Results (14)
More Search Options
Match
Type
Why
Analysis of dystrophin deletion mutations predicts age of cardiomyopathy onset in becker muscular dystrophy.
Academic Article
Why?
Current understanding and management of dilated cardiomyopathy in Duchenne and Becker muscular dystrophy.
Academic Article
Why?
Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms.
Academic Article
Why?
FIOROTTO, MARTA
Person
Why?
Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.
Academic Article
Why?
Quality assurance for Duchenne and Becker muscular dystrophy genetic testing: development of a genomic DNA reference material panel.
Academic Article
Why?
Relation of Cardiac Dysfunction to Rhythm Abnormalities in Patients With Duchenne or Becker Muscular Dystrophies.
Academic Article
Why?
ENG, CHRISTINE
Person
Why?
GASTIER-FOSTER, JULIE
Person
Why?
MIYAKE, CHRISTINA
Person
Why?
LOTZE, TIMOTHY
Person
Why?
PIGNATELLI, RICARDO
Person
Why?
KIM, JEFFREY
Person
Why?
VALDES, SANTIAGO
Person
Why?
Per Page
15
25
50
100
Page
of 1
Next
Prev
Search Criteria
Muscular Dystrophy Duchenne
Becker
Filter by Type
All
(14)
People
(8)
Research
(6)
_
Click "Why?" to see why an item matched the search.