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1Academic Journal
المؤلفون: Paulussen, A DC, Schrander-Stumpel, Connie, Tserpelis, D, Spee, K, Stegmann, Sander, Mancini, Grazia Maria Stefania, Brooks, Alice S, Collée, J M, Maat-Kievit, Anneke, Simon, M EH, Van Bever, Yolande, Stolte-Dijkstra, Irene, Kerstjens-Frederikse, W S, Herkert, J C, Van Essen, Ton J., Lichtenbelt, K D, Van Haeringen, Arie, Kwee, Mei Lan, Lachmeijer, A. M.A., Tan-Sindhunata, M.B., Van Maarle, Merel, Arens, Y H, Smeets, Eric, De Die-Smulders, Christine E.M., Engelen, John J, Smeets, Bert, Herbergs, J
المساهمون: Department of Clinical Genetics
المصدر: ISSN: 1018-4813.
مصطلحات موضوعية: Holoprosencephaly, genotype-phenotype, mutations
Relation: hal-00544822; https://hal.archives-ouvertes.fr/hal-00544822; https://hal.archives-ouvertes.fr/hal-00544822/document; https://hal.archives-ouvertes.fr/hal-00544822/file/PEER_stage2_10.1038%252Fejhg.2010.70.pdf
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2Academic Journal
المؤلفون: Mundlos, Stefan, Kantaputra, Piranit Nik, Klopocki, Eva, Hennig, Bianca P, Le Caignec, Cedric, Praphanphoj, Verayuth, Kwee, Mei Lan, Shears, Deborah J, Isidor, Bertrand
المساهمون: Charité Campus Virchow-Klinikum (CVK)
المصدر: ISSN: 1018-4813.
مصطلحات موضوعية: mesomelic dysplasia Kantaputra type, HOXD, microduplication
Relation: hal-00558093; https://hal.archives-ouvertes.fr/hal-00558093; https://hal.archives-ouvertes.fr/hal-00558093/document; https://hal.archives-ouvertes.fr/hal-00558093/file/PEER_stage2_10.1038%252Fejhg.2010.116.pdf
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3Academic Journal
المؤلفون: Kwee, Mei Lan, Balemans, Wendy, Cleiren, Erna, Gille, Johan JP, Van Der Blij, Frits, Sepers, Jan M, Van Hul, Wim
المصدر: Journal of Bone and Mineral Research ; volume 20, issue 7, page 1254-1260 ; ISSN 0884-0431 1523-4681
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4Academic Journal
المؤلفون: Kroes, Hester Y., van Zon, Patrick H.A., van de Putte, Dietje Fransen, Nelen, Marcel R., Nievelstein, Rutger-Jan, Wittebol-Post, Dienke, van Nieuwenhuizen, Onno, Mancini, Grazia M.S., van der Knaap, Marjo S., Kwee, Mei Lan, Maas, Saskia M., Cobben, Jan Maarten, De Nef, Jacques E.E., Lindhout, Dick, Sinke, Richard J.
المصدر: European Journal of Medical Genetics ; volume 51, issue 1, page 24-34 ; ISSN 1769-7212
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5Academic Journal
المؤلفون: Joenje, Hans, Arwert, Fr�, Kwee, Mei Lan, Madan, Kamlesh, Hoehn, Holger
المصدر: American Journal of Medical Genetics ; volume 79, issue 5, page 403-404 ; ISSN 0148-7299 1096-8628
الاتاحة: http://dx.doi.org/10.1002/(sici)1096-8628(19981012)79:5%3C403::aid-ajmg16%3E3.0.co%3B2-v
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2F(SICI)1096-8628(19981012)79:5%3C403::AID-AJMG16%3E3.0.CO%3B2-V
https://onlinelibrary.wiley.com/doi/full/10.1002/(SICI)1096-8628(19981012)79:5%3C403::AID-AJMG16%3E3.0.CO%3B2-V -
6Academic Journal
المؤلفون: van Dorp, Dieuwke B., Palan, Alzbeta, Kwee, Mei Lan, Barth, Peter G., van der Harten, Johan J.
المصدر: American Journal of Medical Genetics ; volume 40, issue 1, page 100-104 ; ISSN 0148-7299 1096-8628
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7Periodical
المؤلفون: Faivre, Laurence, Guardiola, Philippe, Lewis, Cathryn, Dokal, Inderjeet, Ebell, Wolfram, Zatterale, Ariana, Altay, Cigdem, Poole, Janet, Stones, David, Kwee, Mei Lan, van Weel-Sipman, Margreet, Havenga, Charmaine, Morgan, Neil, de Winter, Johan, Digweed, Martin, Savoia, Anna, Pronk, Jan, de Ravel, Thomas, Jansen, Stander, Joenje, Hans, Gluckman, Eliane, Mathew, Christopher G.
المصدر: Blood; December 2000, Vol. 96 Issue: 13 p4064-4070, 7p
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