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Phenotypic and Functional Consequences of Haploinsufficiency of Genes from Exocyst and Retinoic Acid Pathway Due to a Recurrent Microdeletion of 2P13.2

AuthID
P-006-97J

Author(s)

Wen, J

Lopes, F

Soares, G

Farrell, SA

Nelson, C

Qiao, Y

Martell, S

Badukke, C

Bessa, C

Ylstra, B

Lewis, S

Isoherranen, N

Maciel, P

Rajcan Separovic, E

Document Type

Article

Year published

2013

Published

in ORPHANET JOURNAL OF RARE DISEASES, ISSN: 1750-1172

Volume: 8, Issue: 1, Pages: 100 (12)

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Publication Identifiers

DOI: 10.1186/1750-1172-8-100

Pubmed: 23837398

SCOPUS: 2-s2.0-84879999423

Wos: WOS:000321696700001

Source Identifiers

ISSN: 1750-1172

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Phenotypic and Functional Consequences of Haploinsufficiency of Genes from Exocyst and Retinoic Acid Pathway Due to a Recurrent Microdeletion of 2P13.2

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Phenotypic and Functional Consequences of Haploinsufficiency of Genes from Exocyst and Retinoic Acid Pathway Due to a Recurrent Microdeletion of 2P13.2

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