Your search returned 195 results.

Results
	181.	Moebius' syndrome with unilateral cerebellar hypoplasia. [electronic resource] by Harbord, M G Finn, J P Hall-Craggs, M A Brett, E M Baraitser, M Producer: 19891201 In: Journal of medical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	182.	Alexander's disease: clues to diagnosis. [electronic resource] by Pridmore, C L Baraitser, M Harding, B Boyd, S G Kendall, B Brett, E M Producer: 19930708 In: Journal of child neurology vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	183.	Ataxia, developmental delay and an extensive neuronal migration abnormality in 2 siblings. [electronic resource] by Harbord, M G Boyd, S Hall-Craggs, M A Kendall, B McShane, M A Baraitser, M Producer: 19910404 In: Neuropediatrics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	184.	Central nervous system malformations in Mohr's syndrome. [electronic resource] by Reardon, W Harbord, M G Hall-Craggs, M A Kendall, B Brett, E M Baraitser, M Producer: 19900110 In: Journal of medical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	185.	Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases. [electronic resource] by Collinge, J Poulter, M Davis, M B Baraitser, M Owen, F Crow, T J Harding, A E Producer: 19920110 In: American journal of human genetics vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	186.	Lethal congenital erythroderma: a newly recognised genetic disorder. [electronic resource] by Shield, J P Judge, M R Reardon, W Baraitser, M Nohria, M Malone, M Harper, J I Producer: 19920723 In: Clinical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	187.	Autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS disease. [electronic resource] by Reardon, W Hockey, A Silberstein, P Kendall, B Farag, T I Swash, M Stevenson, R Baraitser, M Producer: 19941129 In: American journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	188.	X-linked recessive bulbospinal neuronopathy: a report of ten cases. [electronic resource] by Harding, A E Thomas, P K Baraitser, M Bradbury, P G Morgan-Hughes, J A Ponsford, J R Producer: 19830214 In: Journal of neurology, neurosurgery, and psychiatry vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	189.	Three patients with the osteochondrodysplasia and hypertrichosis syndrome--Cantu syndrome. [electronic resource] by Rosser, E M Kaariainen, H Hurst, J A Baraitser, M Hall, C M Clayton, P Leonard, J V Producer: 19980710 In: Clinical dysmorphology vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	190.	Craniofacial abnormalities, agenesis of the corpus callosum, polysyndactyly and abnormal skin and gut development--the Curry Jones syndrome. [electronic resource] by Temple, I K Eccles, D M Winter, R M Baraitser, M Carr, S B Shortland, D Jones, M C Curry, C Producer: 19950816 In: Clinical dysmorphology vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	191.	Mesomelic limb shortness: a previously unreported autosomal recessive type. [electronic resource] by Reardon, W Hall, C M Slaney, S Huson, S M Connell, J al-Hilaly, N Fixsen, J Baraitser, M Winter, R M Producer: 19940125 In: American journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	192.	Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes. [electronic resource] by Rutland, P Pulleyn, L J Reardon, W Baraitser, M Hayward, R Jones, B Malcolm, S Winter, R M Oldridge, M Slaney, S F Producer: 19950524 In: Nature genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	193.	Frontonasal dysplasia with optic disc anomalies and other midline craniofacial defects: a report of six cases. [electronic resource] by Lees, M M Hodgkins, P Reardon, W Taylor, D Stanhope, R Jones, B Hayward, R Hockley, A D Baraitser, M Winter, R M Producer: 19981015 In: Clinical dysmorphology vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	194.	Evidence for digenic inheritance in some cases of Antley-Bixler syndrome? [electronic resource] by Reardon, W Smith, A Honour, J W Hindmarsh, P Das, D Rumsby, G Nelson, I Malcolm, S Adès, L Sillence, D Kumar, D DeLozier-Blanchet, C McKee, S Kelly, T McKeehan, W L Baraitser, M Winter, R M Producer: 20000218 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	195.	A gene for FG syndrome maps in the Xq12-q21.31 region. [electronic resource] by Briault, S Hill, R Shrimpton, A Zhu, D Till, M Ronce, N Margaritte-Jeannin, P Baraitser, M Middleton-Price, H Malcolm, S Thompson, E Hoo, J Wilson, G Romano, C Guichet, A Pembrey, M Fontes, M Poustka, A Moraine, C Producer: 19980123 In: American journal of medical genetics vol. 73 Availability: No items available. Save to lists Add to cart (remove)

First
Previous
1
2
3
4
5
6
7
8
9
10