Risk Factors for Hemoptysis in Idiopathic and Hereditary Pulmonary Arterial Hypertension

por Tio, Darryl, Leter, Edward, Boerrigter, Bart, Boonstra, Anco, Vonk-Noordegraaf, Anton, Bogaard, Harm Jan
Publicado 2013

New mutations and an updated database for the patched‐1 (PTCH1) gene

por Reinders, Marie G., van Hout, Antonius F., Cosgun, Betûl, Paulussen, Aimée D., Leter, Edward M., Steijlen, Peter M., Mosterd, Klara, van Geel, Michel, Gille, Johan J.
Publicado 2018

Evaluation of yield and experiences of age‐related molecular investigation for heritable and nonheritable causes of mismatch repair deficient colorectal cancer to identify Lynch sy...

por Vos, Janet R., Fakkert, Ingrid E., Spruijt, Liesbeth, Willems, Riki W., Langenveld, Sera, Mensenkamp, Arjen R., Leter, Edward M., Nagtegaal, Iris D., Ligtenberg, Marjolijn J. L., Hoogerbrugge, Nicoline
Publicado 2020

TBX4 mutations (small patella syndrome) are associated with childhood-onset pulmonary arterial hypertension

por Kerstjens-Frederikse, Wilhelmina S, Bongers, Ernie M H F, Roofthooft, Marcus T R, Leter, Edward M, Douwes, J Menno, Van Dijk, Arie, Vonk-Noordegraaf, Anton, Dijk-Bos, Krista K, Hoefsloot, Lies H, Hoendermis, Elke S, Gille, Johan J P, Sikkema-Raddatz, Birgit, Hofstra, Robert M W, Berger, Rolf M F
Publicado 2013

Universal Tumor DNA BRCA1/2 Testing of Ovarian Cancer: Prescreening PARPi Treatment and Genetic Predisposition

por Vos, Janet R, Fakkert, Ingrid E, de Hullu, Joanne A, van Altena, Anne M, Sie, Aisha S, Ouchene, Hicham, Willems, Riki W, Nagtegaal, Iris D, Jongmans, Marjolijn C J, Mensenkamp, Arjen R, Woldringh, Gwendolyn H, Bulten, Johan, Leter, Edward M, Kets, C Marleen, Simons, Michiel, Ligtenberg, Marjolijn J L, Hoogerbrugge, Nicoline
Publicado 2019