Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Home
Search
Quick Search
Advanced
Fulltext
Browse
Collections
Persons
My eDoc
Session History
Login
Name:
Password:
Documentation
Help
Support Wiki
Direct access to
document ID:


          Display Documents


Institute:
Collection:
Print in Citation style Print version     Display:
Sort by: Display records with Fulltext only
Entries: 1-2  
 Basket 
Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein–Taybi syndrome
Authors: Bartsch, Oliver; Rasi, Sasan; Delicado, Alicia; Dyack, Sarah; Neumann, Luitgard M.; Seemanová, Eva; Volleth, Marianne; Haaf, Thomas; Kalscheuer, Vera M.
Date of Publication (YYYY-MM-DD): 2006-06-17
Title of Journal: Human Genetics
Volume: 120
Issue / Number: 3
Start Page: 179
End Page: 186
Document Type: Article
ID: 307322.0
 
Full text / Content available
Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease
Authors: Bækvad-Hansen, Marie; Tümer, Zeynep; Delicado, Alicia; Erdogan, Fikret; Tommerup, Niels; Larsen, Lars A.
Date of Publication (YYYY-MM-DD): 2006-02-06
Title of Journal: American Journal of Medical Genetics Part A
Volume: 140
Issue / Number: 5
Start Page: 427
End Page: 33
Document Type: Article
ID: 307318.0
 
Full text / Content available
Entries: 1-2  
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.