Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rianne Schaap"'
Autor:
Cornelis L. Harteveld, Ahlem Achour, Sandra J. G. Arkesteijn, Jeanet ter Huurne, Maaike Verschuren, Sharda Bhagwandien‐Bisoen, Rianne Schaap, Linda Vijfhuizen, Hakima el Idrissi, Tamara T. Koopmann
Publikováno v:
International Journal of Laboratory Hematology, 44, 28-36. WILEY
Hemoglobinopathies are the most common monogenic disorders in the world with an ever increasing global disease burden each year. As most hemoglobinopathies show recessive inheritance carriers are usually clinically silent. Programmes for preconceptio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c502b86fee3dee381b0fd10147f47ad
https://hdl.handle.net/1887/3563775
https://hdl.handle.net/1887/3563775
Autor:
Cornelis L. Harteveld, Joanne Traeger-Synodinos, Jennichjen Slomp, Christina Vrettou, Sharda Bisoen, Maaike Verschuren, Nicolette S. den Hollander, Jeanet A.C. ter Huurne, Ahlem Achour, Gijs W. E. Santen, Frédéric Galactéros, Claudia A. L. Ruivenkamp, Rianne Schaap, Rob Castel, Tamara T. Koopmann, Serge Pissard, Sandra G.J. Arkesteijn, Anneliese Grimbergen, Jeroen Knijnenburg, Frank Baas, Linda Vijfhuizen
Publikováno v:
Blood, 136(15), 1789-1793. American Society of Hematology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4225dfea7a09de85bd680889f7293ac
https://pubmed.ncbi.nlm.nih.gov/34854076
https://pubmed.ncbi.nlm.nih.gov/34854076
Autor:
Cornelis L. Harteveld, Sharda Bisoen, Sandra G.J. Arkesteijn, Femke van Erp, Rianne Schaap, Ahlem Achour, Maaike Verschuren, Elke de Grouw, Jeanet A.C. ter Huurne
Publikováno v:
International Journal of Laboratory Hematology, 41, 3, pp. 76-78
International Journal of Laboratory Hematology
International Journal of Laboratory Hematology, 41, 76-78
International Journal of Laboratory Hematology
International Journal of Laboratory Hematology, 41, 76-78
Contains fulltext : 206805.pdf (Publisher’s version ) (Open Access)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de8397ba6b212a54123b11c50914f2b3
http://hdl.handle.net/1887/121747
http://hdl.handle.net/1887/121747
Autor:
Kirsten van Lom, Cornelis L. Harteveld, Ileana Cantú, Rianne Schaap, Sjaak Philipsen, Abdelhafid Natiq, Bella Banjanin, Nynke Gillemans, Abdelaziz Sefiani, Saaid Amzazi, Siham Chafai Elalaoui, Philippe A. Lysy
Publikováno v:
American Journal of Hematology, 92(1), E2-E3. Wiley-Liss Inc.
American Journal of Hematology, 92(1), E2-E3
American Journal of Hematology, 92(1), E2-E3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac277a1810549759ef463109ca4f48f5
https://pure.eur.nl/en/publications/ba8db83e-8f52-4b1e-b58c-af96dd1bc4e0
https://pure.eur.nl/en/publications/ba8db83e-8f52-4b1e-b58c-af96dd1bc4e0
Autor:
Ingrid P. Vogelaar, Cornelis L. Harteveld, Piero C. Giordano, Rianne Schaap, Jeetindra R A Balak, Supan Fucharoen, Attawut Chaibunruang, Egbert Bakker, Johan T. den Dunnen, Marion Phylipsen, Yavuz Ariyurek
Publikováno v:
Human Mutation; Vol 33
Human Mutation, 33(1), 272-280
Human Mutation, 33(1), 272-80
Human Mutation, 33, 272-80
Human Mutation, 33, 1, pp. 272-80
Human Mutation, 33(1), 272-280
Human Mutation, 33(1), 272-80
Human Mutation, 33, 272-80
Human Mutation, 33, 1, pp. 272-80
Item does not contain fulltext Implementation of multiplex ligation-dependent probe amplification (MLPA) for thalassemia causing deletions has lead to the detection of new rearrangements. Knowledge of the exact breakpoint sequences should give more i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77a720926cee880802e09f3002f61d98
Autor:
George L. Boxma, Andrea C. de Bruin-Roest, Willem C. H. Van Helden, Piero C. Giordano, Ingrid P. Vogelaar, Sandra G.J. Arkesteijn, Cornelis L. Harteveld, Rianne Schaap, Marion Phylipsen, Irene C.M. Wildschut
Publikováno v:
Blood Cells, Molecules and Diseases, 45, 2, pp. 133-5
Blood Cells, Molecules and Diseases, 45, 133-5
Blood Cells, Molecules and Diseases
Blood Cells, Molecules and Diseases, 45, 133-5
Blood Cells, Molecules and Diseases
Alpha-thalassemia is an inherited hemoglobin disorder characterized by a microcytic hypochromic anemia caused by a quantitative reduction of the alpha-globin chain. The majority of the alpha-thalassemias is caused by deletions in the alpha-globin gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ab98e76a593a42a3eb1ce028d6e3a38
https://hdl.handle.net/2066/87813
https://hdl.handle.net/2066/87813