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	121.	Congenital cataract, microphthalmia and septal heart defect in two generations: a new syndrome? [electronic resource] by Wilkie, A O Taylor, D Scambler, P J Baraitser, M Producer: 19940217 In: Clinical dysmorphology vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	122.	The clinical features of the Cohen syndrome: further case reports. [electronic resource] by North, C Patton, M A Baraitser, M Winter, R M Producer: 19850619 In: Journal of medical genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	123.	Joubert-Boltshauser syndrome with polydactyly in siblings. [electronic resource] by Egger, J Bellman, M H Ross, E M Baraitser, M Producer: 19821216 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)
	124.	Focal dermal hypoplasia (Goltz syndrome). [electronic resource] by Temple, I K MacDowall, P Baraitser, M Atherton, D J Producer: 19900515 In: Journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	125.	Proteus syndrome: report of a case with severe brain impairment and fatal course. [electronic resource] by Rizzo, R Pavone, L Sorge, G Parano, E Baraitser, M Producer: 19900727 In: Journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	126.	A familial syndrome of microcephaly, sparse hair, mental retardation, and seizures. [electronic resource] by van Haeringen, A Hurst, J A Savidge, R Baraitser, M Producer: 19900507 In: Journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	127.	Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further case. [electronic resource] by Winter, R M Swallow, D M Baraitser, M Purkiss, P Producer: 19810226 In: Clinical genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	128.	Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndrome. [electronic resource] by Reardon, W Gibbons, R J Winter, R M Baraitser, M Producer: 19950525 In: American journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	129.	Oculofacialbulbar palsy in mother and son: review of 26 reports of familial transmission within the 'Möbius spectrum of defects'. [electronic resource] by MacDermot, K D Winter, R M Taylor, D Baraitser, M Producer: 19910411 In: Journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	130.	Pitfalls in counselling: the craniosynostoses. [electronic resource] by Marini, R Temple, K Chitty, L Genet, S Baraitser, M Producer: 19910412 In: Journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	131.	The iris in Williams syndrome. [electronic resource] by Holmström, G Almond, G Temple, K Taylor, D Baraitser, M Producer: 19901107 In: Archives of disease in childhood vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	132.	Natural history, symptoms and treatment of the narcoleptic syndrome. [electronic resource] by Parkes, J D Baraitser, M Marsden, C D Asselman, P Producer: 20091211 In: Acta neurologica Scandinavica vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	133.	Perlman and Wiedemann-Beckwith syndromes: two distinct conditions associated with Wilms' tumour. [electronic resource] by Grundy, R G Pritchard, J Baraitser, M Risdon, A Robards, M Producer: 19930204 In: European journal of pediatrics vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	134.	Two brothers with heart defects and limb shortening: case reports and review. [electronic resource] by Reardon, W Hurst, J Farag, T I Hall, C Baraitser, M Producer: 19910412 In: Journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	135.	An oculocerebral hypopigmentation syndrome: a case report with clinical, histochemical, and ultrastructural findings. [electronic resource] by Patton, M A Baraitser, M Heagerty, A H Eady, R A Producer: 19870520 In: Journal of medical genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	136.	Selective IgG2 subclass deficiency--a marker for the syndrome of pre/postnatal growth retardation, developmental delay, hypotrophy of distal extremities, dental anomalies and eczema. [electronic resource] by Ainsworth, S B Baraitser, M Mueller, R F Massey, R F Producer: 19970707 In: Clinical dysmorphology vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	137.	Pelizaeus-Merzbacher disease: detection of mutations Thr181----Pro and Leu223----Pro in the proteolipid protein gene, and prenatal diagnosis. [electronic resource] by Strautnieks, S Rutland, P Winter, R M Baraitser, M Malcolm, S Producer: 19921028 In: American journal of human genetics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	138.	Midline facial defects with ocular colobomata. [electronic resource] by Temple, I K Brunner, H Jones, B Burn, J Baraitser, M Producer: 19901205 In: American journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	139.	Rapadilino syndrome--a non-Finnish case. [electronic resource] by Kant, S G Baraitser, M Milla, P J Winter, R M 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)
	140.	Intrafamilial correlation in Friedreich's ataxia. [electronic resource] by Winter, R M Harding, A E Baraitser, M Bravery, M B Producer: 19820621 In: Clinical genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 195 results.