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Interstitial 22q13 deletions not involving SHANK3 gene: a new contiguous gene syndrome
- Disciglio, V (author)
- Lo Rizzo, C (author)
- Mencarelli, MA (author)
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- Mucciolo, M (author)
- Marozza, A (author)
- Di Marco, C (author)
- Massarelli, A (author)
- Canocchi, V (author)
- Baldassarri, M (author)
- Ndoni, E (author)
- Frullanti, E (author)
- Amabile, S (author)
- Metcalfe, K (author)
- Le Caignec, C (author)
- David, A (author)
- Fryer, A (author)
- Boute, O (author)
- Joris, A (author)
- Greco, D (author)
- Pecile, V (author)
- Battini, R (author)
- Novelli, A (author)
- Fichera, M (author)
- Romano, C (author)
- Mari, F (author)
- Renieri, A (author)
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- (creator_code:org_t)
- 2014-04-03
- 2014
- English.
- In: American journal of medical genetics. Part A. - : Wiley. - 1552-4833 .- 1552-4825. ; 164164A:7, s. 1666-1676
- Journal article (peer-reviewed)
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- American journal of medical genetics. Part A (Search for host publication in LIBRIS)
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- Disciglio, V
- Lo Rizzo, C
- Mencarelli, MA
- Mucciolo, M
- Marozza, A
- Di Marco, C
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- Massarelli, A
- Canocchi, V
- Baldassarri, M
- Ndoni, E
- Frullanti, E
- Amabile, S
- Anderlid, BM
- Metcalfe, K
- Le Caignec, C
- David, A
- Fryer, A
- Boute, O
- Joris, A
- Greco, D
- Pecile, V
- Battini, R
- Novelli, A
- Fichera, M
- Romano, C
- Mari, F
- Renieri, A
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- Karolinska Institutet
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