Dual genetic diagnoses: neurofibromatosis type 1 and KBG syndrome. Issue 2 (April 2020)
- Record Type:
- Journal Article
- Title:
- Dual genetic diagnoses: neurofibromatosis type 1 and KBG syndrome. Issue 2 (April 2020)
- Main Title:
- Dual genetic diagnoses
- Authors:
- Cianci, Paola
Pezzoli, Laura
Maitz, Silvia
Agosti, Massimo
Iascone, Maria
Selicorni, Angelo - Abstract:
- Is Part Of:
- Clinical dysmorphology. Volume 29:Issue 2(2020:Apr.)
- Journal:
- Clinical dysmorphology
- Issue:
- Volume 29:Issue 2(2020:Apr.)
- Issue Display:
- Volume 29, Issue 2 (2020)
- Year:
- 2020
- Volume:
- 29
- Issue:
- 2
- Issue Sort Value:
- 2020-0029-0002-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-04
- Subjects:
- Abnormalities, Human -- Periodicals
Genetic disorders -- Periodicals
Abnormalities -- periodicals
Abnormalities, Human
Periodicals
616.042 - Journal URLs:
- http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=00019605-000000000-00000 ↗
http://journals.lww.com/clindysmorphol/pages/default.aspx ↗
http://journals.lww.com/pages/default.aspx ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1097/MCD.0000000000000296 ↗
- Languages:
- English
- ISSNs:
- 0962-8827
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.273700
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 18728.xml