A Novel Rad21 Variant in Family with Mild Cornelia de Lange Syndrome Phenotype

AuthID
P-00T-878
5
Author(s)
Grangeia, A
·
Alonso, I
·
Santos, H
·
Leao, M
Document Type
Abstract
Year published
2020
Published
in MEDICINE, ISSN: 0025-7974
Volume: 99, Issue: 9
Conference
23Rd Annual Meeting of the Portuguese-Society-Of-Human-Genetics, Date: NOV 14-16, 2019, Location: Coimbra, PORTUGAL, Sponsors: Portuguese Soc Human Genet
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Publication Identifiers
Wos: WOS:000525865600157
Source Identifiers
ISSN: 0025-7974
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