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Ploos van Amstel, J. K.
157
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1
SMAD4gene mutation increases the risk of aortic dilation in..:
Vorselaars, V.M.M.
;
Diederik, A.
;
Prabhudesai, V.
...
International Journal of Cardiology. 245 (2017) - p. 114-118 , 2017
Link:
https://doi.org/10.1016/..
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2
Unexplained False Negative Results in Noninvasive Prenatal ..:
Hochstenbach, R.
;
Page-Christiaens, G. C. M. L.
;
van Oppen, A. C. C.
...
Case Reports in Genetics. 2015 (2015) - p. 1-7 , 2015
Link:
https://doi.org/10.1155/..
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3
1028 ALPHA FETOPROTEIN (AFP): A CONFOUNDING FACTOR IN UROLO..:
Houwert, A.C.
;
Giltay, J.C.
;
Ploos Van Amstel, J.K.
..
European Urology Supplements. 10 (2011) 2 - p. 318-319 , 2011
Link:
https://doi.org/10.1016/..
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4
Influence of the type of F8 gene mutation on inhibitor deve..:
GOUW, S. C.
;
VAN DER BOM, J. G.
;
VAN DEN BERG, H. M.
...
Haemophilia. 17 (2010) 2 - p. 275-281 , 2010
Link:
https://doi.org/10.1111/..
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5
P11: Loci of shared segmental aneuploidy in the genomes of ..:
Poot, Martin
;
Eleveld, M.J.
;
Ploos van Amstel, J.K.
.
European Journal of Medical Genetics. 48 (2005) 4 - p. 455 , 2005
Link:
https://doi.org/10.1016/..
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6
Rapid detection of chromosomal aneuploidies in uncultured a..:
Hochstenbach, R.
;
Meijer, J.
;
van de Brug, J.
...
Prenatal Diagnosis. 25 (2005) 11 - p. 1032-1039 , 2005
Link:
https://doi.org/10.1002/..
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7
P20: Improving Whole Genome Amplification methods for pre-i..:
Nilsson, P.R.
;
Knijnenburg, J.
;
Gutknecht, D.R.
...
European Journal of Medical Genetics. 48 (2005) 4 - p. 465 , 2005
Link:
https://doi.org/10.1016/..
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8
Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutati..:
Letteboer, T. G. W.
;
Zewald, R. A.
;
Kamping, E. J.
...
Human Genetics. 116 (2004) 1-2 - p. 8-16 , 2004
Link:
https://doi.org/10.1007/..
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9
Earliest gestational age for fetal sexing in cell‐free mate..:
Rijnders, R. J. P.
;
Van Der Luijt, R. B.
;
Peters, E. D. J.
...
Prenatal Diagnosis. 23 (2003) 13 - p. 1042-1044 , 2003
Link:
https://doi.org/10.1002/..
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10
Isolated and contiguous glycerol kinase gene disorders: A r..:
Sjarif, D. R.
;
Ploos van Amstel, J. K.
;
Duran, M.
..
Journal of Inherited Metabolic Disease. 23 (2000) 6 - p. 529-547 , 2000
Link:
https://doi.org/10.1023/..
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11
Different phenotypic expression in relatives with Fabry dis..:
Knol, I.E.
;
Ausems, M.G.E.M.
;
Lindhout, D.
...
American Journal of Medical Genetics. 82 (1999) 5 - p. 436-439 , 1999
Link:
https://doi.org/10.1002/..
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12
The multiple cases of Fabry disease in a Russian family cau..:
Beyer, E.M
;
Karpova, E.A
;
Udalova, O.V
...
Clinica Chimica Acta. 280 (1999) 1-2 - p. 81-89 , 1999
Link:
https://doi.org/10.1016/..
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13
Experiences of bereaved family caregivers with shared decis..:
van Oosterhout, Sanne P. C.
;
Ermers, Daisy J. M.
;
Ploos van Amstel, Floor K.
...
BMC Palliative Care. 20 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
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14
Does a regular nurse‐led distress screening and discussion ..:
Ploos van Amstel, Floortje K.
;
Peters, Marlies E. W. J.
;
Donders, Rogier
...
Psycho-Oncology. 29 (2020) 4 - p. 719-728 , 2020
Link:
https://doi.org/10.1002/..
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15
The clinical and genetic features of hereditary haemorrhagi..:
Mutize, Tendaishe T.
;
Seedat, Riaz Y.
;
Ploos van Amstel, Johannes K.
...
Molecular Biology Reports. 47 (2020) 12 - p. 9967-9972 , 2020
Link:
https://doi.org/10.1007/..
1-15