Results
|
21.
|
|
|
22.
|
|
|
23.
|
|
|
24.
|
|
|
25.
|
|
|
26.
|
|
|
27.
|
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3. [electronic resource] by
- Lesperance, M M
- Hall, J W
- Bess, F H
- Fukushima, K
- Jain, P K
- Ploplis, B
- San Agustin, T B
- Skarka, H
- Smith, R J
- Wills, M
Producer: 19960418
In:
Human molecular genetics vol. 4
Availability: No items available.
|
|
28.
|
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus. [electronic resource] by
- Van Camp, G
- Kunst, H
- Flothmann, K
- McGuirt, W
- Wauters, J
- Marres, H
- Verstreken, M
- Bespalova, I N
- Burmeister, M
- Van de Heyning, P H
- Smith, R J
- Willems, P J
- Cremers, C W
- Lesperance, M M
Producer: 19990831
In:
Journal of medical genetics vol. 36
Availability: No items available.
|
|
29.
|
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. [electronic resource] by
- Bespalova, I N
- Van Camp, G
- Bom, S J
- Brown, D J
- Cryns, K
- DeWan, A T
- Erson, A E
- Flothmann, K
- Kunst, H P
- Kurnool, P
- Sivakumaran, T A
- Cremers, C W
- Leal, S M
- Burmeister, M
- Lesperance, M M
Producer: 20020221
In:
Human molecular genetics vol. 10
Availability: No items available.
|
|
30.
|
Differential Proteomics for Distinguishing Ischemic Stroke from Controls: a Pilot Study of the SpecTRA Project. [electronic resource] by
- Penn, A M
- Saly, V
- Trivedi, A
- Lesperance, M L
- Votova, K
- Jackson, A M
- Croteau, N S
- Balshaw, R F
- Bibok, M B
- Smith, D S
- Lam, K K
- Morrison, J
- Lu, L
- Coutts, S B
- Borchers, C H
Producer: 20181211
In:
Translational stroke research vol. 9
Availability: No items available.
|