WFRF:(Huang L.)
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Subtelomeric deletions of chromosome 9q: a novel microdeletion syndrome
- Stewart, DR (author)
- Huang, A (author)
- Faravelli, F (author)
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- Medne, L (author)
- Ciprero, K (author)
- Kaur, M (author)
- Rossi, E (author)
- Tenconi, R (author)
- Gripp, KW (author)
- Nicholson, L (author)
- Meschino, WS (author)
- Capua, E (author)
- Quarrell, OWJ (author)
- Flint, J (author)
- Irons, M (author)
- Giampietro, PF (author)
- Schowalter, DB (author)
- Zaleski, CA (author)
- Malacarne, M (author)
- Zackai, EH (author)
- Spinner, NB (author)
- Krantz, ID (author)
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- (creator_code:org_t)
- 2004-07-14
- 2004
- English.
- In: American journal of medical genetics. Part A. - : Wiley. - 1552-4825. ; 128A:4, s. 340-351
- Journal article (peer-reviewed)
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- Stewart, DR
- Huang, A
- Faravelli, F
- Anderlid, BM
- Medne, L
- Ciprero, K
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- Kaur, M
- Rossi, E
- Tenconi, R
- Nordenskjold, M
- Gripp, KW
- Nicholson, L
- Meschino, WS
- Capua, E
- Quarrell, OWJ
- Flint, J
- Irons, M
- Giampietro, PF
- Schowalter, DB
- Zaleski, CA
- Malacarne, M
- Zackai, EH
- Spinner, NB
- Krantz, ID
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- Karolinska Institutet
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