Home
About
Overview
Sharing Data
ORCID
Help
History (18)
Mutations in the glucokinase gene are not a major cause of late-onset type 2 (non-insulin-dependent) diabetes mellitus in Japanese subjects.
An inventory of our therapeutic possessions.
The "megalencephaly-capillary malformation" (MCAP) syndrome: the nomenclature of a highly recognizable multiple congenital anomaly syndrome.
Allogeneic transplantation for AML and MDS: GVL versus GVHD and disease recurrence.
Comprehensive molecular diagnostics in autosomal dominant polycystic kidney disease.
See All 18 Pages
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
Comprehensive molecular diagnostics in autosomal dominant polycystic kidney disease.
Comprehensive molecular diagnostics in autosomal dominant polycystic kidney disease. J Am Soc Nephrol. 2007 Jul; 18(7):2143-60.
View in:
PubMed
subject areas
Adolescent
Adult
Humans
Middle Aged
Molecular Diagnostic Techniques
Mutation
Polycystic Kidney, Autosomal Dominant
Sequence Analysis, DNA
authors with profiles
Arlene Chapman