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	1.	Three Mendelian disorders (chronic granulomatous disease, retinitis pigmentosa, ornithine transcarbamylase deficiency) in a young woman with an X chromosome deletion, del(X)(p11.4p21.1). [electronic resource] by Coman, David Yaplito-Lee, Joy La, Phung Nasioulas, Steven Bruno, Damien Slater, Howard R Stock-Myer, Sharyn E Lynch, Elly L Gardner, R J McKinlay Producer: 20100518 In: Molecular genetics and metabolism vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro. [electronic resource] by Natesan, Senthilkumar A Bladon, Alex J Coskun, Serdar Qubbaj, Wafa Prates, Renata Munne, Santiago Coonen, Edith Dreesen, Joseph C F M Stevens, Servi J C Paulussen, Aimee D C Stock-Myer, Sharyn E Wilton, Leeanda J Jaroudi, Souraya Wells, Dagan Brown, Anthony P C Handyside, Alan H Producer: 20150706 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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