|
🐜
|
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
19 auth.
R. Birkenhäger,
E. Otto,
M. Schürmann,
M. Vollmer,
Eva-Maria Ruf,
Irina Maier-Lutz,
Frank Beekmann,
Andrea Fekete,
H. Omran,
D. Feldmann,
...
D. Milford,
N. Jeck,
M. Konrad,
D. Landau,
N. Knoers,
C. Antignac,
R. Sudbrak,
A. Kispert,
F. Hildebrandt
|
8 |
2001 |
8
🐜
|
|
🐜
|
Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3.
10 auth.
U. Finckh,
S. Xu,
GOVINDASAMY KUMARAMANICKAVEL,
M. Schürmann,
J. Mukkadan,
S. Fernandez,
...
S. John,
J. Weber,
M. Denton,
A. Gal
|
5 |
1998 |
5
🐜
|
|
🐬
|
Analysis of aberrant human Y chromosomes by recombinant DNA probes
J. Arnemann,
S. Jakubiczka,
C. Fonatsch,
M. Schürmann,
D. Probeck,
J. Schmidtke
|
0 |
1986 |
0
🐬
|
