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Browsing "Paediatrics publications" by Author Bain, S.

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Showing results 1 to 7 of 7

Preview	Issue Date	Title	Author(s)
	2003	Acute lymphoblastic leukemia characterized by t(8;14)(q11.2;q32)	Moore, S.; Suttle, J.; Bain, S.; Story, C.; Rice, M.
	2013	Epilepsy with cognitive deficit and autism spectrum disorders: Prospective diagnosis by array CGH	Nicholl, J.; Waters, W.; Suwalski, S.; Brown, S.; Hull, Y.; Harbord, M.; Entwistle, J.; Thompson, S.; Clark, D.; Pridmore, C.; Haan, E.; Barnett, C.; McGregor, L.; Liebelt, J.; Thompson, E.; Friend, K.; Bain, S.; Yu, S.; Mulley, J.
	2008	Familial 22q11.2 duplication: a three-generation family with a 3-Mb duplication and a familial 1.5-Mb duplication	Yu, S.; Cox, K.; Friend, K.; Smith, S.; Buchheim, R.; Bain, S.; Leibelt, J.; Thompson, E.; Bratkovic, D.
	2010	Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3	Heron, S.; Scheffer, I.; Grinton, B.; Eyre, H.; Oliver, K.; Bain, S.; Berkovic, S.; Mulley, J.
	1997	High resolution characterisation of an interstitial deletion of less than 1.9Mb at 4p16.3 associated with Wolf-Hirschhorn Syndrome	Fang, Y.; Bain, S.; Haan, E.; Eyre, H.; MacDonald, M.; Wright, T.; Altherr, M.; Riess, O.; Sutherland, G.; Callen, D.
	2011	Inherited Balanced Translocation t(9;17)(q33.2;q25.3) Concomitant With a 16p13.1 Duplication in a Patient With Schizophrenia	Fullston, T.; Gabb, B.; Callen, D.; Ullmann, R.; Woollatt, E.; Bain, S.; Ropers, H.; Cooper, M.; Chandler, D.; Carter, K.; Jablensky, A.; Kalaydjieva, L.; Gecz, J.
	2005	Unstable Robertsonian translocations der(13;15)(q10;q10): Heritable chromosome fission without phenotypic effect in two kindreds	Perry, J.; White, S.; Nouri, S.; Bain, S.; Hutchinson, R.; La, P.; Northrop, E.; Eyre, H.; Pertile, M.; Hocking, T.; Thompson, E.; Yu, S.; Choo, K.; Slater, H.

Showing results 1 to 7 of 7