Epilepsy with cognitive deficit and autism spectrum disorders: Prospective diagnosis by array CGH
Nicholl, Jillian, Waters, Wendy, Suwalski, Shanna, Brown, Sue, Hull, Yvonne, Harbord, Michael G., Entwistle, John, Thompson, Suzanna, Clark, Damian, Pridmore, Claire, Haan, Eric, Barnett, Christopher, McGregor, Lesley, Liebelt, Jan, Thompson, Elizabeth M., Friend, Kathryn, Bain, Sharon M., Yu, Sui, Mulley, John C.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.01.2013)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.01.2013)
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Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH
Nicholl, Jillian, Waters, Wendy, Mulley, John C., Suwalski, Shanna, Brown, Sue, Hull, Yvonne, Barnett, Christopher, Haan, Eric, Thompson, Elizabeth M., Liebelt, Jan, Mcgregor, Lesley, Harbord, Michael G., Entwistle, John, Munt, Chris, White, Dierdre, Chitti, Anthony, Baulderstone, David, Ketteridge, David, Friend, Kathryn, Bain, Sharon M., Sui, Y.u.
Published in Pathology (01.01.2014)
Published in Pathology (01.01.2014)
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Gene expression analysis in absence epilepsy using a monozygotic twin design
Helbig, Ingo, Matigian, Nicholas A., Vadlamudi, Lata, Lawrence, Kate M., Bayly, Marta A., Bain, Sharon M., Diyagama, Dileepa, Scheffer, Ingrid E., Mulley, John C., Holloway, Andrew J., Dibbens, Leanne M., Berkovic, Samuel F., Hayward, Nicholas K.
Published in Epilepsia (Copenhagen) (01.09.2008)
Published in Epilepsia (Copenhagen) (01.09.2008)
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Unstable Robertsonian translocations der(13;15)(q10;q10): Heritable chromosome fission without phenotypic effect in two kindreds
Perry, Jo, White, Sue M., Nouri, Sara, Bain, Sharon M., Hutchinson, Rhonda G., La, Phung, Northrop, Emma, Eyre, Helen J., Pertile, Mark D., Hocking, Trudy A., Thompson, Elizabeth M., Yu, Sui, Choo, K.H. Andy, Slater, Howard R.
Published in American journal of medical genetics. Part A (01.07.2005)
Published in American journal of medical genetics. Part A (01.07.2005)
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