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Entries: 1-3  
A clinical and molecular genetic study of 112 Iranian families with primary microcephaly.
Authors: Darvish, H. .; Nieh, Sahar Esmaeeli; Monajemi, G. B.; Mohseni, M.; Ghasemi-Firouzabadi, S.; Abedini, S. S.; Bahman, I.; P Jamali, P.; Azimi, S.; Mojahedi, F.; Dehghan, A.; Shafeghati, Y.; Jankhah, A.; Falah, M.; Soltani Banavandi, M. J.; Ghani-Kakhi, M.; Garshasbi, M.; Rakhshani, F.; Naghavi, A.; Tzschach, Andreas; Neitzel, H.; Ropers, Hans-Hilger; Kuss, Andreas W.; Behjati, F.; Kahrizi, K.; Najmabadi, Hossein
Date of Publication (YYYY-MM-DD): 2010-10-26
Title of Journal: Journal of Medical Genetics.
Volume: 47
Issue / Number: 12
Start Page: 823
End Page: 828
Document Type: Article
ID: 532565.0
Full text / Content available
Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotype.
Authors: Dutrannoy, V.; Demuth, I.; Baumann, U.; Schindler, D.; Konrat, K.; Neitzel, H.; Gillessen-Kaesbach, G.; Radszewski, J.; Rothe, S.; Schellenberger, M. T.; Nurnberg, G.; Nurnberg, P.; Teik, K. W.; Nallusamy, R.; Reis, A.; Sperling, K.; Digweed, M.; Varon, R.
Date of Publication (YYYY-MM-DD): 2010-07-01
Title of Journal: Human Mutation
Volume: 31
Issue / Number: 9
Start Page: 1059
End Page: 1068
Document Type: Article
ID: 539705.0
Copy and paste: the impact of a new non-L1 retroposon on the gonosomal heterochromatin of Microtus agrestis
Authors: Neitzel, H.; Kalscheuer, V.; Singh, A. P.; Henschel, S.; Sperling, K.
Date of Publication (YYYY-MM-DD): 2002
Title of Journal: Cytogenetic and Genome Research
Volume: 96
Issue / Number: 1-4
Start Page: 179
End Page: 185
Document Type: Article
ID: 24244.0
Entries: 1-3  
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