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Terminal deletion of Xp22.3 associated with contiguous gene syndrome: Leri-Weill dyschondrosteosis, developmental delay, and ichthyosis

Title
Terminal deletion of Xp22.3 associated with contiguous gene syndrome: Leri-Weill dyschondrosteosis, developmental delay, and ichthyosis
Type
Another Publication in an International Scientific Journal
Year
2001
Authors
Vassal, H
(Author)
Other
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Medeira, A
(Author)
Other
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Cordeiro, I
(Author)
Other
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Santos, HG
(Author)
Other
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CASTEDO, S
(Author)
FMUP
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Saraiva, C
(Author)
Other
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da Silva, PM
(Author)
Other
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Monteiro, C
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Journal
Vol. 99
Pages: 331-334
ISSN: 0148-7299
Publisher: Wiley
Other information
Authenticus ID: P-000-VW8
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 4
Documents
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