Results
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7301.
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7302.
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7303.
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Deletion mapping of 22q11 in CATCH22 syndrome: identification of a second critical region. [electronic resource] by
- Kurahashi, H
- Nakayama, T
- Osugi, Y
- Tsuda, E
- Masuno, M
- Imaizumi, K
- Kamiya, T
- Sano, T
- Okada, S
- Nishisho, I
Producer: 19960725
In:
American journal of human genetics vol. 58
Availability: No items available.
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7304.
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7305.
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7306.
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7307.
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7308.
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7309.
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7310.
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7311.
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7312.
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7313.
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7314.
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7315.
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7316.
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7317.
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7318.
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Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group. [electronic resource] by
- Lopes, J
- LeGuern, E
- Gouider, R
- Tardieu, S
- Abbas, N
- Birouk, N
- Gugenheim, M
- Bouche, P
- Agid, Y
- Brice, A
Producer: 19960725
In:
American journal of human genetics vol. 58
Availability: No items available.
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7319.
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7320.
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