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Ploos van Amstel, J. K.
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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/..
 
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