Please note that eDoc will be permanently shut down in the first quarter of 2021!      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: 1-5  
 Basket 
Hypergonadotropic hypogonadism in a patient with inv ins (2;4)
Authors: Tzschach, A.; Ramel, C.; Kron, A.; Seipel, B.; Wüster, C.; Cordes, U.; Liehr, T.; Hoeltzenbein, M.; Menzel, C.; Ropers, H.-H.; Ullmann, R.; Kalscheuer, V.; Decker, J.; Steinberger, D.
Date of Publication (YYYY-MM-DD): 2009-06
Title of Journal: International Journal of Andrology
Volume: 32
Issue / Number: 3
Start Page: 226
End Page: 230
Document Type: Article
ID: 473660.0
Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation
Authors: Erdogan, F.; Chen, W.; Kirchhoff, M.; Kalscheuer, V. M.; Hultschig, C.; Müller, I.; Schulz, A.; Menzel, C.; Bryndorf, T.; Ropers, H.-H.; Ullmann, R.
Date of Publication (YYYY-MM-DD): 2006-11
Title of Journal: Cytogenetic and Genome Research
Volume: 115
Issue / Number: 3-4
Start Page: 247
End Page: 253
Document Type: Article
ID: 307491.0
Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation
Authors: Erdogan, F.; Chen, W.; Kirchhoff, M.; Kalscheuer, V. M.; Hultschig, C.; Müller, I.; Schulz, A.; Menzel, C.; Bryndorf, T.; Ropers, H.-H.; Ullmann, R.
Date of Publication (YYYY-MM-DD): 2006-11
Title of Journal: Cytogenetic and Genome Research
Volume: 115
Issue / Number: 3-4
Start Page: 247
End Page: 253
Document Type: Article
ID: 307610.0
Discrimination between Alzheimer dementia and controls by automated analysis of multicenter FDG PET
Authors: Herholz, Karl; Salmon, E.; Perani, D.; Baron, J. C.; Holthoff, Vjera; Frölich, L.; Schönknecht, P.; Ito, K.; Mielke, Rüdiger; Kalbe, Elke; Zündorf, Gerhard; Delbeuck, X.; Pelati, O.; Anchisi, D.; Fazio, F.; Kerrouche, N.; Desgranges, B.; Eustache, F.; Beuthien-Baumann, B.; Menzel, C.; Schröder, J.; Kato, T.; Arahata, Y.; Henze, M.; Heiss, Wolf-Dieter
Date of Publication (YYYY-MM-DD): 2002-09
Title of Journal: NeuroImage
Volume: 17
Issue / Number: 1
Start Page: 302
End Page: 316
Document Type: Article
ID: 13606.0
A cryptic deletion of 2q35 including part of the PAX3
gene detected by breakpoint mapping in a child with
autism and a de novo 2;8 translocation
Authors: Borg, I.; Squire, M.; Menzel, C.; Stout, K.; Morgan, D.; Willatt, L.; O’Brien, P. C. M.; Ferguson-Smith, M. A.; Ropers, Hans Hilger; Tommerup, N.; Kalscheuer, Vera M.; Sargan, D. R.
Date of Publication (YYYY-MM-DD): 2002-06
Title of Journal: Journal of Medical Genetics
Volume: 39
Issue / Number: 6
Start Page: 391
End Page: 399
Document Type: Article
ID: 24147.0
Entries: 1-5  
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.