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Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells
by
Bliek, Jet
,
Alders, Marielle
,
Maas, Saskia M
,
Oostra, Roelof-Jan
,
Mackay, Deborah M
,
van der Lip, Karin
,
Callaway, Johnatan L
,
Brooks, Alice
,
van 't Padje, Sandra
,
Westerveld, Andries
,
Leschot, Nico J
,
Mannens, Marcel MAM
Published in
European journal of human genetics : EJHG
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Characterisation of Fmrp in zebrafish: evolutionary dynamics of the fmr1 gene
by
van 't Padje, Sandra
,
Engels, Bart
,
Blonden, Lau
,
Severijnen, Lies-Anne
,
Verheijen, Frans
,
Oostra, Ben A
,
Willemsen, Rob
Published in
Development genes and evolution
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Transport kinetics of FMRP containing the I304N mutation of severe fragile X syndrome in neurites of living rat PC12 cells
by
Schrier, Mariëtte
,
Severijnen, Lies-Anne
,
Reis, Surya
,
Rife, Maria
,
van't Padje, Sandra
,
van Cappellen, Gert
,
Oostra, Ben A.
,
Willemsen, Rob
Published in
Experimental neurology
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Development Genes And Evolution
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Fragile X Mental Retardation Protein
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Beckwith-Wiedemann Syndrome
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