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	1.	The use of arrays to detect copy-number variations in clinical practice. [electronic resource] by Sikkema-Raddatz, Birgit Sijmons, Rolf H Producer: 20120906 In: Human mutation vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent. [electronic resource] by Dondorp, Wybo Sikkema-Raddatz, Birgit de Die-Smulders, Christine de Wert, Guido Producer: 20120906 In: Human mutation vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Targeted next-generation sequencing panels for monogenetic disorders in clinical diagnostics: the opportunities and challenges. [electronic resource] by de Koning, Tom J Jongbloed, Jan D H Sikkema-Raddatz, Birgit Sinke, Richard J Producer: 20160223 In: Expert review of molecular diagnostics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: report on two patients and review of the literature. [electronic resource] by Raas-Rothschild, Annick Dijkhuizen, Trijnie Sikkema-Raddatz, Birgit Werner, Marion Dagan, Judith Abeliovich, Devorah Lerer, Israela Producer: 20090901 In: European journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Genome-wide arrays in routine diagnostics of hematological malignancies. [electronic resource] by Simons, Annet Sikkema-Raddatz, Birgit de Leeuw, Nicole Konrad, Nicole Claudia Hastings, Rosalind J Schoumans, Jacqueline Producer: 20120906 In: Human mutation vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Temporal and developmental-stage variation in the occurrence of mitotic errors in tripronuclear human preimplantation embryos. [electronic resource] by Mantikou, Eleni van Echten-Arends, Jannie Sikkema-Raddatz, Birgit van der Veen, Fulco Repping, Sjoerd Mastenbroek, Sebastiaan Producer: 20131023 In: Biology of reproduction vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Madelung deformity in a girl with a novel and de novo mutation in the GNAS gene. [electronic resource] by Rump, Patrick Jongbloed, Jan D H Sikkema-Raddatz, Birgit Mundlos, Stefan Klopocki, Eva van der Luijt, Rob B Producer: 20120118 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Quality aspects of prenatal cytogenetic diagnosis: determining the effect of various factors involved in handling amniotic fluid and chorionic villus material for cytogenetic diagnosis. [electronic resource] by Sikkema-Raddatz, Birgit Suijkerbuijk, Ron Bouman, Katelijne de Jong, Bauke Buys, Charles H C M te Meerman, Gerard J Producer: 20061228 In: Prenatal diagnosis vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	An absolute procedure to test the growth potential of medium and the influence of decreased oxygen tension in primary amniotic fluid cell cultures. [electronic resource] by Sikkema-Raddatz, Birgit Suijkerbuijk, Ron van der Vlag, Jakob Stoepker, Marian Buys, Charles H C M te Meerman, Gerard J Producer: 20061228 In: Prenatal diagnosis vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Chromosomal mosaicism in human preimplantation embryos: a systematic review. [electronic resource] by van Echten-Arends, Jannie Mastenbroek, Sebastiaan Sikkema-Raddatz, Birgit Korevaar, Johanna C Heineman, Maas Jan van der Veen, Fulco Repping, Sjoerd Producer: 20111213 In: Human reproduction update vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	A unique 970kb microdeletion in 9q33.3, including the NR5A1 gene in a 46,XY female. [electronic resource] by van Silfhout, Anneke Boot, Annemieke M Dijkhuizen, Trijnie Hoek, Annemieke Nijman, Rien Sikkema-Raddatz, Birgit van Ravenswaaij-Arts, Conny M A Producer: 20090901 In: European journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Array analysis and karyotyping: workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands. [electronic resource] by Hochstenbach, Ron van Binsbergen, Ellen Engelen, John Nieuwint, Aggie Polstra, Abeltje Poddighe, Pino Ruivenkamp, Claudia Sikkema-Raddatz, Birgit Smeets, Dominique Poot, Martin Producer: 20091102 In: European journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion. [electronic resource] by Gerkes, Erica H Hordijk, Roel Dijkhuizen, Trijnie Sival, Deborah A Meiners, Linda C Sikkema-Raddatz, Birgit van Ravenswaaij-Arts, Conny M A Producer: 20110111 In: European journal of medical genetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	A 649 kb microduplication in 1p34.1, including POMGNT1, in a patient with microcephaly, coloboma and laryngomalacia; and a review of the literature. [electronic resource] by Hanemaaijer, Nicolien Dijkhuizen, Trijnie Haadsma, Maaike Boeve, Margot Boon, Maartje Hordijk, Roel Kok, Klaas Sikkema-Raddatz, Birgit van Ravenswaaij-Arts, Conny M A Producer: 20090901 In: European journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Haploinsufficiency of the STX1B gene is associated with myoclonic astatic epilepsy. [electronic resource] by Vlaskamp, Danique R M Rump, Patrick Callenbach, Petra M C Vos, Yvonne J Sikkema-Raddatz, Birgit van Ravenswaaij-Arts, Conny M A Brouwer, Oebele F Producer: 20161213 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	A novel homozygous insertion and review of published mutations in the NNT gene causing familial glucocorticoid deficiency (FGD). [electronic resource] by Jazayeri, Omid Liu, Xuanzhu van Diemen, Cleo C Bakker-van Waarde, Willie M Sikkema-Raddatz, Birgit Sinke, Richard J Zhang, Jianguo van Ravenswaaij-Arts, Conny M A Producer: 20161011 In: European journal of medical genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	The introduction of arrays in prenatal diagnosis: a special challenge. [electronic resource] by Vetro, Annalisa Bouman, Katelijne Hastings, Ros McMullan, Dominic J Vermeesch, Joris R Miller, Konstantin Sikkema-Raddatz, Birgit Ledbetter, David H Zuffardi, Orsetta van Ravenswaaij-Arts, Conny M A Producer: 20120906 In: Human mutation vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Split hand/foot malformation due to chromosome 7q aberrations(SHFM1): additional support for functional haploinsufficiency as the causative mechanism. [electronic resource] by van Silfhout, Anneke T van den Akker, Peter C Dijkhuizen, Trijnie Verheij, Joke B G M Olderode-Berends, Maran J W Kok, Klaas Sikkema-Raddatz, Birgit van Ravenswaaij-Arts, Conny M A Producer: 20100112 In: European journal of human genetics : EJHG vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	FISH and array-CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions. [electronic resource] by Dijkhuizen, Trijnie van Essen, Ton van der Vlies, Pieter Verheij, Joke B G M Sikkema-Raddatz, Birgit van der Veen, Anneke Y Gerssen-Schoorl, Klasien B J Buys, Charles H C M Kok, Klaas Producer: 20070112 In: American journal of medical genetics. Part A vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome. [electronic resource] by Willemsen, Marjolein H Fernandez, Bridget A Bacino, Carlos A Gerkes, Erica de Brouwer, Arjan P M Pfundt, Rolph Sikkema-Raddatz, Birgit Scherer, Stephen W Marshall, Christian R Potocki, Lorraine van Bokhoven, Hans Kleefstra, Tjitske Producer: 20100629 In: European journal of human genetics : EJHG vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 39 results.