File Download

There are no files associated with this item.

Supplementary

Book Chapter: A 1.36-megabase deletion in chromosome 18q21.32 including GRP in a patient with epilepsy, borderline intellectual disability, and multiple cerebral cavernous malformations

TitleA 1.36-megabase deletion in chromosome 18q21.32 including GRP in a patient with epilepsy, borderline intellectual disability, and multiple cerebral cavernous malformations
Authors
Baum, LGuo, YGui, HSham, PCCherny, SSKwan, P
Issue Date2015
PublisherNova Science
Citation
A 1.36-megabase deletion in chromosome 18q21.32 including GRP in a patient with epilepsy, borderline intellectual disability, and multiple cerebral cavernous malformations. In Waye, MMY (Ed.), Biochemistry and Molecular Biology: The Complexity of Human Traits and Diseases, p. 37-46. Hauppauge, NY: Nova Science, 2015 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/226407
ISBN
978-1-63482-312-8
Series/Report no.Biochemistry research trends series

 

DC FieldValueLanguage
dc.contributor.authorBaum, L-
dc.contributor.authorGuo, Y-
dc.contributor.authorGui, H-
dc.contributor.authorSham, PC-
dc.contributor.authorCherny, SS-
dc.contributor.authorKwan, P-
dc.date.accessioned2016-06-17T07:43:58Z-
dc.date.available2016-06-17T07:43:58Z-
dc.date.issued2015-
dc.identifier.citationA 1.36-megabase deletion in chromosome 18q21.32 including GRP in a patient with epilepsy, borderline intellectual disability, and multiple cerebral cavernous malformations. In Waye, MMY (Ed.), Biochemistry and Molecular Biology: The Complexity of Human Traits and Diseases, p. 37-46. Hauppauge, NY: Nova Science, 2015-
dc.identifier.isbn978-1-63482-312-8-
dc.identifier.urihttp://hdl.handle.net/10722/226407-
dc.languageeng-
dc.publisherNova Science-
dc.relation.ispartofBiochemistry and Molecular Biology: The Complexity of Human Traits and Diseases-
dc.relation.ispartofseriesBiochemistry research trends series-
dc.titleA 1.36-megabase deletion in chromosome 18q21.32 including GRP in a patient with epilepsy, borderline intellectual disability, and multiple cerebral cavernous malformations-
dc.typeBook_Chapter-
dc.identifier.emailSham, PC: pcsham@hku.hk-
dc.identifier.emailCherny, SS: cherny@hku.hk-
dc.identifier.authoritySham, PC=rp00459-
dc.identifier.authorityCherny, SS=rp00232-
dc.identifier.hkuros258287-
dc.identifier.spage37-
dc.identifier.epage46-
dc.publisher.placeHauppauge, NY-

Export via OAI-PMH Interface in XML Formats

OR

Export to Other Non-XML Formats