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1 Ergebnisse
1
Heterozygous lamin B1 and lamin B2 variants cause primary m..:
Parry, DA
;
Martin, C-A
;
Greene, P
...
Genet Med. , 2020
Link:
https://qmro.qmul.ac.uk/xmlui/handle/123456789/70067
RT Journal T1
Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy
UL https://suche.suub.uni-bremen.de/peid=base-ftqueenmaryuniv:oai:qmro.qmul.ac.uk:123456789_70067&Exemplar=1&LAN=DE A1 Parry, DA A1 Martin, C-A A1 Greene, P A1 Marsh, JA A1 Genomics England Research Consortium A1 Blyth, M A1 Cox, H A1 Donnelly, D A1 Greenhalgh, L A1 Greville-Heygate, S A1 Harrison, V A1 Lachlan, K A1 McKenna, C A1 Quigley, AJ A1 Rea, G A1 Robertson, L A1 Suri, M A1 Jackson, AP YR 2020 K1 LMNB1 K1 LMNB2 K1 laminopathy K1 neurodevelopmental disorder K1 primary microcephaly JF Genet Med LK http://dx.doi.org/https://qmro.qmul.ac.uk/xmlui/handle/123456789/70067 DO https://qmro.qmul.ac.uk/xmlui/handle/123456789/70067 SF ELIB - SuUB Bremen
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