Novel variation in ANTXR2 gene causing hyaline fibromatosis syndrome: A report from India. (23rd March 2021)

Record Type:: Journal Article
Title:: Novel variation in ANTXR2 gene causing hyaline fibromatosis syndrome: A report from India. (23rd March 2021)
Main Title:: Novel variation in ANTXR2 gene causing hyaline fibromatosis syndrome: A report from India
Authors:: Chaudhry, Chakshu
Kaur, Parminder
Srivastava, Priyanka
Panigrahi, Inusha
Kaur, Anupriya
Abstract:
Is Part Of:: Congenital anomalies. Volume 61:Number 4(2021)
Journal:: Congenital anomalies
Issue:: Volume 61:Number 4(2021)
Issue Display:: Volume 61, Issue 4 (2021)
Year:: 2021
Volume:: 61
Issue:: 4
Issue Sort Value:: 2021-0061-0004-0000
Page Start:: 140
Page End:: 141
Publication Date:: 2021-03-23
Subjects:: Abnormalities, Human -- Periodicals
616.043
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/loi/cga ↗
DOI:: 10.1111/cga.12414 ↗
Languages:: English
ISSNs:: 0914-3505
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3410.683000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 17454.xml