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Partially methylated alleles, microdeletion, and tissue mosaicism in a fragile X male with tremor and ataxia at 30 years of age: a case report

- Hwang, Yun Tae, Aliaga, Solange Mabel, Heard, Robert, Godler, David Eugeny, Arpone, Marta, Francis, David, Li, Xin, Chong, Belinda, Slater, Howard Robert, Rogers, Carolyn, Bretherton, Lesley, Hunter, Matthew

Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families

- Hynes, Kim, Tarpey, Patrick, Haan, Eric, Turner, Gillian, Christodoulou, John, Leonard, Helen, Gill, Deepak, Stratton, Michael R., Gecz, Jozef, Scheffer, Ingrid E., Dibbens, Leanne M., Bayly, Marta A., Berkovic, Samuel F., Smith, Raffaella, Al Raisi, Zahyia, Turner, Samantha J., Brown, Natasha J., Desai, Tarishi D.

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

- Tarpey, Patrick S., Smith, Raffaella, Stephens, Phil, Blow, Matt, Greenman, Chris, Xue, Yali, Tyler-Smith, Chris, Thompson, Deborah, Gray, Kristian, Andrews, Jenny, Barthorpe, Syd, Buck, Gemma, Pleasance, Erin, Hackett, Anna, Whibley, Annabel, Edkins, Sarah, Hardy, Claire, O'Meara, Sarah, Latimer, Calli, Dicks, Ed, Menzies, Andrew

Atypical Angelman syndrome with macrocephaly due to a familial imprinting center deletion

- Ronan, Anne, Buiting, Karin, Dudding, Tracy

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