W. S. Kerstjens-Frederikse

发表

W. Timens, J. V. van Montfrans, M. Hennus, 2021, Orphanet Journal of Rare Diseases.

M. Weiss, A. Balk, M. Slegtenhorst, 2010, Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation.

R. Hofstra, C. Buys, A. V. van Essen, 1999, Journal of medical genetics.

R. Berger, W. S. Kerstjens-Frederikse, M. Haarman, 2020, Current opinion in pulmonary medicine.

R. Groen, J. V. van Dijk, M. ter Laan, 2009, Twin Research and Human Genetics.

E. Bongers, L. Hoefsloot, R. Hofstra, 2013, Journal of Medical Genetics.

J. Roos‐Hesselink, F. Meijboom, P. Pieper, 2005, Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation.

R. Hofstra, T. Plösch, R. Berger, 2013, Biology of reproduction.

B. D. de Vries, M. P. van den Berg, Patrick Deelen, 2021, European Journal of Human Genetics.

L. Hoefsloot, C. V. van Ravenswaaij-Arts, G. J. du Marchie Sarvaas, 2014, American journal of medical genetics. Part A.

H. Smeets, A. Paulussen, A. Haeringen, 2010, European Journal of Human Genetics.

Marilyn C. Jones, T. Glover, M. McDonald, 2001, Journal of medical genetics.

C. V. van Ravenswaaij-Arts, K. Abbott, W. S. Kerstjens-Frederikse, 2022, European Journal of Human Genetics.

R. Hofstra, D. Lütjohann, T. Plösch, 2012, American journal of obstetrics and gynecology.

M. Nóbrega, T. Meitinger, M. Lathrop, 2021, Circulation research.

C. V. van Ravenswaaij-Arts, T. Dijkhuizen, N. Corsten-Janssen, 2022, Orphanet Journal of Rare Diseases.

Cleo C. van Diemen, Birgit Sikkema-Raddatz, Kristin M. Abbott, 2019, Genome Medicine.

K. Heimdal, R. Hennekam, L. Hoefsloot, 2013, Circulation. Cardiovascular genetics.

H. Hillege, W. Timens, Y. Vos, 2020, The Journal of pediatrics.

M. Reijnders, W. Chung, A. Munnich, 2020, Genetics in Medicine.

R. Sinke, J. P. van Tintelen, A. Pósafalvi, 2011, Expert opinion on medical diagnostics.

B. D. de Vries, J. Roos‐Hesselink, A. Bertoli-Avella, 2009, American journal of medical genetics. Part A.

E. Zackai, L. Hoefsloot, B. Emanuel, 2013, Molecular Syndromology.

H. Smeets, T. de Ravel, K. Devriendt, 2011, Human mutation.

Cleo C. van Diemen, M. Swertz, K. J. van der Velde, 2021, Frontiers in Pediatrics.

Birgit Sikkema-Raddatz, Pieter B. T. Neerincx, Morris A Swertz, 2017, Pediatrics.

M. Swertz, C. V. van Ravenswaaij-Arts, A. Ranchor, 2022, Orphanet Journal of Rare Diseases.

R. Berger, W. S. Kerstjens-Frederikse, M. Haarman, 2019, European Respiratory Journal.

S. Nik-Zainal, K. Devriendt, R. Hennekam, 2008, Human mutation.

A. Pagnamenta, Jenny C. Taylor, K. Abbott, 2021, Clinical genetics.

Y. Pinto, J. Osinga, M. P. van den Berg, 2007, Journal of the American College of Cardiology.

B. Leegte, A. V. van Essen, W. S. Kerstjens-Frederikse, 1999, Genetic counseling.

C. Cytrynbaum, T. Scheidl, B. Emanuel, 1997, Journal of medical genetics.

Wilhelmina S Kerstjens-Frederikse, L. de Jong-van den Berg, C. Buys, 2009, Birth defects research. Part A, Clinical and molecular teratology.

Eva Corpeleijn, Wilhelmina S Kerstjens-Frederikse, R. Hofstra, 2014 .

Willemijn M. Meijer, Wilhelmina S Kerstjens-Frederikse, L. de Jong-van den Berg, 2005, Reproductive toxicology.

M. Swertz, C. V. van Ravenswaaij-Arts, T. Dijkhuizen, 2022, Orphanet Journal of Rare Diseases.

Y. Pinto, R. Tio, J. P. van Tintelen, 2010, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.

R. Hofstra, J. Christodoulou, C. Bole-Feysot, 2020, American journal of human genetics.

R. Hofstra, J. Roos‐Hesselink, K. Lichtenbelt, 2014 .

F. Dikkers, W. S. Kerstjens-Frederikse, P. H. Robinson, 2003, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

F. Dikkers, W. S. Kerstjens-Frederikse, P. H. Robinson, 2003 .

M. Swertz, R. Sinke, L. Franke, 2022 .