Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro
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
Published in Genetics in medicine (01.11.2014)
Published in Genetics in medicine (01.11.2014)
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Journal Article
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)
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
Published in Molecular genetics and metabolism (01.03.2010)
Published in Molecular genetics and metabolism (01.03.2010)
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Journal Article
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)
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
Published in Molecular genetics and metabolism (01.03.2010)
Published in Molecular genetics and metabolism (01.03.2010)
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