MPPH syndrome with aortic coarctation and macrosomia due to CCND2 mutations. Issue 1 (19th January 2020)

Record Type:: Journal Article
Title:: MPPH syndrome with aortic coarctation and macrosomia due to CCND2 mutations. Issue 1 (19th January 2020)
Main Title:: MPPH syndrome with aortic coarctation and macrosomia due to CCND2 mutations
Authors:: Sameshima, Tomohiro
Morisada, Naoya
Egawa, Tsuyoshi
Kugo, Masaaki
Iijima, Kazumoto
Abstract:
Is Part Of:: Pediatrics international. Volume 62:Issue 1(2020)
Journal:: Pediatrics international
Issue:: Volume 62:Issue 1(2020)
Issue Display:: Volume 62, Issue 1 (2020)
Year:: 2020
Volume:: 62
Issue:: 1
Issue Sort Value:: 2020-0062-0001-0000
Page Start:: 115
Page End:: 117
Publication Date:: 2020-01-19
Subjects:: aortic coarctation -- CCND2 -- hydrocephalus -- MPPH syndrome -- postaxial polydactyly
Pediatrics -- Periodicals
618.92
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1442-200X/issues. Subscription to online journal required for access to full text. ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/ped.14068 ↗
Languages:: English
ISSNs:: 1328-8067
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 6417.655800
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Ingest File:: 12643.xml