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Refining the 9q34.3 microduplication syndrome reveals mild ..:
Rots, Dmitrijs
;
Rooney, Kathleen
;
Relator, Raissa
...
Clinical Genetics. 105 (2024) 6 - p. 655-660 , 2024
Link:
https://doi.org/10.1111/cge.14498
RT Journal T1
Refining the 9q34.3 microduplication syndrome reveals mild neurodevelopmental features associated with a distinct global DNA methylation profile
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.14498&Exemplar=1&LAN=DE A1 Rots, Dmitrijs A1 Rooney, Kathleen A1 Relator, Raissa A1 Kerkhof, Jennifer A1 McConkey, Haley A1 Pfundt, Rolph A1 Marcelis, Carlo A1 Willemsen, Marjolein H. A1 van Hagen, Johanna M. A1 Zwijnenburg, Petra A1 Alders, Marielle A1 Õunap, Katrin A1 Reimand, Tiia A1 Fjodorova, Olga A1 Berland, Siren A1 Liahjell, Eva Benedicte A1 Bojovic, Ognjen A1 Kriek, Marjolein A1 Ruivenkamp, Claudia A1 Bonati, Maria Teresa A1 Brunner, Han G. A1 Vissers, Lisenka E. L. M. A1 Sadikovic, Bekim A1 Kleefstra, Tjitske PB Wiley YR 2024 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 105 IS 6 SP 655 OP 660 LK http://dx.doi.org/https://doi.org/10.1111/cge.14498 DO https://doi.org/10.1111/cge.14498 SF ELIB - SuUB Bremen
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