-
1
-
-
0034641596
-
Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome
-
Bondurand N., Pingault V., Goerich D.E., Lemort N., Sock E., Le Caignec C., Wegner M., Goosens M. (2000) Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome. Hum. Mol. Genet., 9, 1907 1917.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1907-1917
-
-
Bondurand, N.1
Pingault, V.2
Goerich, D.E.3
Lemort, N.4
Sock, E.5
Le Caignec, C.6
Wegner, M.7
Goosens, M.8
-
2
-
-
0034181460
-
Complex segregation analysis of deafness in Dalmatian dogs
-
Famula T.R., Oberbauer A.M., Sousa C.A. (2000) Complex segregation analysis of deafness in Dalmatian dogs. Am. J. Vet. Res., 61, 550 553.
-
(2000)
Am. J. Vet. Res.
, vol.61
, pp. 550-553
-
-
Famula, T.R.1
Oberbauer, A.M.2
Sousa, C.A.3
-
3
-
-
0041382658
-
Analysis of systematic effects on congenital sensorineural deafness in German Dalmatian dogs
-
Juraschko K., Meyer-Lindenberg A., Nolte I., Distl O. (2003a) Analysis of systematic effects on congenital sensorineural deafness in German Dalmatian dogs. Vet. J., 166, 164 169.
-
(2003)
Vet. J.
, vol.166
, pp. 164-169
-
-
Juraschko, K.1
Meyer-Lindenberg, A.2
Nolte, I.3
Distl, O.4
-
4
-
-
0042816527
-
A regressive model analysis of congenital sensorineural deafness in German Dalmatian dogs
-
Juraschko K., Meyer-Lindenberg A., Nolte I., Distl O. (2003b) A regressive model analysis of congenital sensorineural deafness in German Dalmatian dogs. Mamm. Genome, 14, 547 554.
-
(2003)
Mamm. Genome
, vol.14
, pp. 547-554
-
-
Juraschko, K.1
Meyer-Lindenberg, A.2
Nolte, I.3
Distl, O.4
-
5
-
-
35648953308
-
Efficient mapping of mendelian traits in dogs through genome-wide association
-
Karlsson E.K., Baranowska I., Wade C.M., Salmon Hillbertz N.H., Zody M.C., Anderson N., Biagi T.M., Patterson N., Pielberg G.R., Kulbokas E.J. III., Comstock K.E., Keller E.T., Mesirov J.P., von Euler H., Kämpe O., Hedhammar A., Lander E.S., Andersson G., Andersson L., Lindblad-Toh K. (2007) Efficient mapping of mendelian traits in dogs through genome-wide association. Nat. Genet., 39, 1304 1306.
-
(2007)
Nat. Genet.
, vol.39
, pp. 1304-1306
-
-
Karlsson, E.K.1
Baranowska, I.2
Wade, C.M.3
Salmon Hillbertz, N.H.4
Zody, M.C.5
Anderson, N.6
Biagi, T.M.7
Patterson, N.8
Pielberg, G.R.9
Kulbokas Iii., E.J.10
Comstock, K.E.11
Keller, E.T.12
Mesirov, J.P.13
Von Euler, H.14
Kämpe, O.15
Hedhammar, A.16
Lander, E.S.17
Andersson, G.18
Andersson, L.19
Lindblad-Toh, K.20
more..
-
7
-
-
0036559631
-
Further contributions to the genetic aspect of congenital sensorineural deafness in Dalmatians
-
Muhle A.C., Jaggy A., Stricker C., Steffen F., Dolf G., Busato A., Kornberg M., Mariscoli M., Srenk P., Gaillard C. (2002) Further contributions to the genetic aspect of congenital sensorineural deafness in Dalmatians. Vet. J., 163, 311 318.
-
(2002)
Vet. J.
, vol.163
, pp. 311-318
-
-
Muhle, A.C.1
Jaggy, A.2
Stricker, C.3
Steffen, F.4
Dolf, G.5
Busato, A.6
Kornberg, M.7
Mariscoli, M.8
Srenk, P.9
Gaillard, C.10
-
8
-
-
14044265170
-
Congenital sensorineural deafness in dogs: A molecular genetic approach toward unravelling the responsible genes
-
Rak S.G., Distl O. (2005) Congenital sensorineural deafness in dogs: a molecular genetic approach toward unravelling the responsible genes. Vet. J., 169, 188 196.
-
(2005)
Vet. J.
, vol.169
, pp. 188-196
-
-
Rak, S.G.1
Distl, O.2
-
9
-
-
33751217430
-
Association of MITF with white spotting in Beagle crosses and Newfoundland dogs
-
Rothschild M.F., Van Cleave P.S., Glenn K.L., Carlstrom L.P., Ellinwood N.M. (2006) Association of MITF with white spotting in Beagle crosses and Newfoundland dogs. Anim. Genet., 37, 606 607.
-
(2006)
Anim. Genet.
, vol.37
, pp. 606-607
-
-
Rothschild, M.F.1
Van Cleave, P.S.2
Glenn, K.L.3
Carlstrom, L.P.4
Ellinwood, N.M.5
-
10
-
-
0347983804
-
Deafness prevalence and pigmentation and gender associations in dog breeds at risk
-
Strain G.M. (2004) Deafness prevalence and pigmentation and gender associations in dog breeds at risk. Vet. J., 167, 23 32.
-
(2004)
Vet. J.
, vol.167
, pp. 23-32
-
-
Strain, G.M.1
-
11
-
-
0343245112
-
A syndrome of deaf-mutism associated with albinism showing dominant autosomal inheritance
-
Tietz W. (1963) A syndrome of deaf-mutism associated with albinism showing dominant autosomal inheritance. Am. J. Hum. Genet., 15, 259 264.
-
(1963)
Am. J. Hum. Genet.
, vol.15
, pp. 259-264
-
-
Tietz, W.1
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