Results
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25881.
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25882.
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25883.
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The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy. [electronic resource] by
- MacKenzie, A E
- Korneluk, R G
- Zorzato, F
- Fujii, J
- Phillips, M
- Iles, D
- Wieringa, B
- Leblond, S
- Bailly, J
- Willard, H F
Producer: 19900621
In:
American journal of human genetics vol. 46
Availability: No items available.
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25884.
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25885.
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25886.
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25887.
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25888.
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25889.
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25890.
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25891.
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25892.
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25893.
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25894.
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25895.
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DNA-based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1). [electronic resource] by
- Järvelä, I
- Rapola, J
- Peltonen, L
- Puhakka, L
- Vesa, J
- Ammälä, P
- Salonen, R
- Ryynänen, M
- Haring, P
- Mustonen, A
Producer: 19911024
In:
Prenatal diagnosis vol. 11
Availability: No items available.
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25896.
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25897.
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25898.
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25899.
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DNA duplication associated with Charcot-Marie-Tooth disease type 1A. [electronic resource] by
- Lupski, J R
- de Oca-Luna, R M
- Slaugenhaupt, S
- Pentao, L
- Guzzetta, V
- Trask, B J
- Saucedo-Cardenas, O
- Barker, D F
- Killian, J M
- Garcia, C A
- Chakravarti, A
- Patel, P I
Producer: 19910827
In:
Cell vol. 66
Availability: No items available.
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25900.
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