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M. Männamaa
M. Männamaa
Tartu University Hospital
Genetics
FOXP2 Gene
Family medicine
Biology
university hospital
2
Papers
68
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Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families
2012
American Journal of Medical Genetics Part A
Olga Zilina
Tiia Reimand
P. Zjablovskaja
Katrin Männik
M. Männamaa
A. Traat
H. Puusepp-Benazzouz
Ants Kurg
Katrin Õunap
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Citations (26)
The screening of SLC6A8 deficiency among Estonian families with X-linked mental retardation
2010
Journal of Inherited Metabolic Disease
H. Puusepp
K. Kall
Gajja S. Salomons
Inga Talvik
M. Männamaa
Reet Rein
C. Jakobs
Katrin Õunap
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Citations (42)
1