Results
|
41.
|
|
|
42.
|
|
|
43.
|
|
|
44.
|
|
|
45.
|
|
|
46.
|
|
|
47.
|
|
|
48.
|
|
|
49.
|
|
|
50.
|
|
|
51.
|
|
|
52.
|
|
|
53.
|
|
|
54.
|
|
|
55.
|
Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation. [electronic resource] by
- Bykhovskaya, Y
- Shohat, M
- Ehrenman, K
- Johnson, D
- Hamon, M
- Cantor, R M
- Aouizerat, B
- Bu, X
- Rotter, J I
- Jaber, L
- Fischel-Ghodsian, N
Producer: 19990205
In:
American journal of medical genetics vol. 77
Availability: No items available.
|
|
56.
|
|
|
57.
|
|
|
58.
|
|
|
59.
|
Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locus. [electronic resource] by
- Bateman, J B
- Kojis, T L
- Cantor, R M
- Heinzmann, C
- Ngo, J T
- Spence, M A
- Inana, G
- Kivlin, J D
- Curtis, D
- Sparkes, R S
Producer: 19940426
In:
Transactions of the American Ophthalmological Society vol. 91
Availability: No items available.
|
|
60.
|
The Tay-Sachs disease gene in North American Jewish populations: geographic variations and origin. [electronic resource] by
- Petersen, G M
- Rotter, J I
- Cantor, R M
- Field, L L
- Greenwald, S
- Lim, J S
- Roy, C
- Schoenfeld, V
- Lowden, J A
- Kaback, M M
Producer: 19840107
In:
American journal of human genetics vol. 35
Availability: No items available.
|