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 
Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation.
Authors: Lugtenberg, Dorien; Zangrande-Vieira, Luiz; Kirchhoff, Maria; Whibley, Annabel C.; Oudakker, Astrid R.; Kjaergaard, Susanne; Vianna-Morgante, Angela M.; Kleefstra, Tjitske; Ruiter, Mariken; Jehee, Fernanda S.; Ullmann, Reinhard; Schwartz, Charles E.; Stratton, Michael; Raymond, F. Lucy; Veltman, Joris A.; Vrijenhoek, Terry; Pfundt, Rolph; Schuurs-Hoeijmakers, Janneke H.M.; Hehir-Kwa, Jayne Y.; Froyen, Guy; Chelly, Jamel; Ropers, Hans-Hilger; Moraine, Claude; Gècz, Jozef; Knijnenburg, Jeroen; Kant, Sarina G.; Hamel, Ben C.J.; Rosenberg, Carla; van Bokhoven, Hans; de Brouwer, Arjan P.M.
Date of Publication (YYYY-MM-DD): 2010-02-10
Title of Journal: American Journal of Medical Genetics. Part A.
Volume: 152A
Issue / Number: 3
Start Page: 638
End Page: 645
Document Type: Article
ID: 533727.0
 
Full text / Content available
Molecular characterization of two patients with de novo interstitial deletions in 4q22-q24
Authors: Hilhorst-Hofstee, Yvonne; Tümer, Zeynep; Born, Peter; Knijnenburg, Jeroen; Hansson, Kerstin; Yatawara, Vindhya; Steensberg, Jesper; Ullmann, Reinhard; Arkesteijn, Ger; Tommerup, Niels; Larsen, Lars Allan
Date of Publication (YYYY-MM-DD): 2009-09
Title of Journal: American Journal of Medical Genetics Part A
Volume: 149
Issue / Number: 8
Start Page: 1830
End Page: 1833
Document Type: Article
ID: 472549.0
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.