Terminal Deletion of Xp22.3 Associated with Contiguous Gene Syndrome: Leri-Weill Dyschondrosteosis, Developmental Delay, and Ichthyosis

AuthID
 P-000-VW8
8
Author(s)
Vassal, H
·
Medeira, A
·
Cordeiro, I
·
Saraiva, C
·
da Silva, PM
·
Monteiro, C
Tipo de Documento
Letter
Year published
2001
Publicado
in AMERICAN JOURNAL OF MEDICAL GENETICS, ISSN: 0148-7299
Volume: 99, Número: 4, Páginas: 331-334 (4)
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Publication Identifiers
Pubmed: 11252003
SCOPUS: 2-s2.0-0035313902
Wos: WOS:000167594800014
Source Identifiers
ISSN: 0148-7299
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