Expanding the Pre- and Postnatal Phenotype of Washc5 and Ccdc22-Related Ritscher-Schinzel Syndromes

AuthID
 P-00X-8XA
11
Author(s)
Neri, S
·
Fortuna, AM
·
Coale, E
·
Willis, M
·
Jorge, P
·
Hojte, AF
·
Fenger, CD
·
Moller, RS
·
Bayat, A
Tipo de Documento
Article
Year published
2022
Publicado
in EUROPEAN JOURNAL OF MEDICAL GENETICS, ISSN: 1769-7212
Volume: 65, Número: 11, Páginas: 104624 (7)
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Publication Identifiers
Pubmed: 36130690
SCOPUS: 2-s2.0-85138187030
Wos: WOS:000929709600012
Source Identifiers
ISSN: 1769-7212
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