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	1.	Re: polymicrogyria versus pachygyria in 22q11 microdeletion. [electronic resource] by de Wit, Marie Claire Y Lequin, Maarten H de Coo, René F M Mancini, Grazia M S Producer: 20050822 In: American journal of medical genetics. Part A vol. 136A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Muscle weakness as presenting symptom of osteogenesis imperfecta. [electronic resource] by Boot, Annemieke M de Coo, Rene F M Pals, Gerard de Muinck Keizer-Schrama, Sabine M P F Producer: 20070608 In: European journal of pediatrics vol. 165 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Molybdenum cofactor deficiency: Identification of a patient with homozygote mutation in the MOCS3 gene. [electronic resource] by Huijmans, Jan G M Schot, Rachel de Klerk, Johannis B C Williams, Monique de Coo, René F M Duran, Marinus Verheijen, Frans W van Slegtenhorst, Marjon Mancini, Grazia M S Producer: 20171201 In: American journal of medical genetics. Part A vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Benign familial infantile convulsions: a clinical study of seven Dutch families. [electronic resource] by Callenbach, Petra M C de Coo, René F M Vein, Alla A Arts, Willem Frans M Oosterwijk, Jan Hageman, Gerard ten Houten, Robert Terwindt, Gisela M Lindhout, Dick Frants, Rune R Brouwer, Oebele F Producer: 20021219 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Familial partial epilepsy with variable foci in a Dutch family: clinical characteristics and confirmation of linkage to chromosome 22q. [electronic resource] by Callenbach, Petra M C van den Maagdenberg, Arn M J M Hottenga, Jouke J van den Boogerd, Eelke H de Coo, René F M Lindhout, Dick Frants, Rune R Sandkuijl, Lodewijk A Brouwer, Oebele F Producer: 20031125 In: Epilepsia vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Aortic distensibility alterations in adults with m.3243A>G MELAS gene mutation. [electronic resource] by Nemes, Attila Geleijnse, Marcel L Sluiter, Wim Vydt, Tom C G Soliman, Osama I I van Dalen, Bas M Vletter, Wim B ten Cate, Folkert J Smeets, Hubert J M de Coo, René F M Producer: 20090413 In: Swiss medical weekly vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Regional absence of mitochondria causing energy depletion in the myocardium of muscle LIM protein knockout mice. [electronic resource] by van den Bosch, Bianca J C van den Burg, Caroline M M Schoonderwoerd, Kees Lindsey, Patrick J Scholte, Hans R de Coo, René F M van Rooij, Eva Rockman, Howard A Doevendans, Pieter A Smeets, Hubert J M Producer: 20050302 In: Cardiovascular research vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Cardiac involvement in adults with m.3243A>G MELAS gene mutation. [electronic resource] by Vydt, Tom C G de Coo, René F M Soliman, Osama I I Ten Cate, Folkert J van Geuns, Robert-Jan M Vletter, Wim B Schoonderwoerd, Kees van den Bosch, Bianca J C Smeets, Hubert J M Geleijnse, Marcel L Producer: 20070227 In: The American journal of cardiology vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Non-random mtDNA segregation patterns indicate a metastable heteroplasmic segregation unit in m.3243A>G cybrid cells. [electronic resource] by Raap, Anton K Jahangir Tafrechi, Roshan S van de Rijke, Frans M Pyle, Angela Wählby, Carolina Szuhai, Karoly Ravelli, Raimond B G de Coo, René F M Rajasimha, Harsha K Nilsson, Mats Chinnery, Patrick F Samuels, David C Janssen, George M C Producer: 20130610 In: PloS one vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background. [electronic resource] by Hudson, Gavin Carelli, Valerio Spruijt, Liesbeth Gerards, Mike Mowbray, Catherine Achilli, Alessandro Pyle, Angela Elson, Joanna Howell, Neil La Morgia, Chiara Valentino, Maria Lucia Huoponen, Kirsi Savontaus, Marja-Liisa Nikoskelainen, Eeva Sadun, Alfredo A Salomao, Solange R Belfort, Rubens Griffiths, Philip Yu-Wai-Man, Patrick de Coo, Rene F M Horvath, Rita Zeviani, Massimo Smeets, Hubert J T Torroni, Antonio Chinnery, Patrick F Producer: 20070921 In: American journal of human genetics vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)