MAPPING OF 2 HEREDITARY RENAL TUBULAR DISORDERS ASSOCIATED WITH KIDNEY-STONES, AND REFERRED TO AS DENT-DISEASE AND X-LINKED RECESSIVE NEPHROLITHIASIS, TO CHROMOSOME-XP11
Hlavní autoři: | Thakker, R, Pang, J, Wooding, C, Scheinman, S, Wrong, O, Pook, M |
---|---|
Médium: | Journal article |
Vydáno: |
1994
|
Podobné jednotky
-
Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.
Autor: Scheinman, S, a další
Vydáno: (1993) -
LOCALIZATION OF THE GENE CAUSING X-LINKED RECESSIVE NEPHROLITHIASIS TO THE SHORT ARM OF THE X-CHROMOSOME (XP11.22)
Autor: Scheinman, S, a další
Vydáno: (1992) -
THE GENE CAUSING DENTS DISEASE, A RENAL FANCONI SYNDROME WITH NEPHROCALCINOSIS AND KIDNEY-STONES, IS ON THE SHORT ARM OF THE X-CHROMOSOME (XP11.22)
Autor: Thakker, R, a další
Vydáno: (1993) -
Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.
Autor: Pook, M, a další
Vydáno: (1993) -
HEREDITARY NEPHROLITHIASIS IS ASSOCIATED WITH MUTATIONS IN AN X-LINKED CHLORIDE CHANNEL GENE
Autor: Lloyd, S, a další
Vydáno: (1995)