Your search returned 195 results.

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	141.	PEHO or PEHO-like syndrome? [electronic resource] by Chitty, L S Robb, S Berry, C Silver, D Baraitser, M Producer: 19960927 In: Clinical dysmorphology vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	142.	The autosomal dominant syndrome with congenital stapes ankylosis, broad thumbs and hyperopia. [electronic resource] by Hilhorst-Hofstee, Y Watkin, P M Hall, C M Baraitser, M Producer: 19970922 In: Clinical dysmorphology vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	143.	An extended family with a dominantly inherited speech disorder. [electronic resource] by Hurst, J A Baraitser, M Auger, E Graham, F Norell, S Producer: 19900604 In: Developmental medicine and child neurology vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	144.	An apparently new syndrome of bowed tibiae, radial anomalies, osteopenia, multiple fractures and developmental delay. [electronic resource] by Chitty, L S Hall, C M Webb, P J Baraitser, M Producer: 19940218 In: Clinical dysmorphology vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	145.	Proteus syndrome: an expanded phenotype. [electronic resource] by Clark, R D Donnai, D Rogers, J Cooper, J Baraitser, M Producer: 19870724 In: American journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	146.	Tel Hashomer camptodactyly syndrome: report of a case with myopathic features. [electronic resource] by Patton, M A McDermot, K D Lake, B D Baraitser, M Producer: 19860725 In: Journal of medical genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	147.	Severe microcephaly, choreiform movements, cataracts and sensorineural deafness in two patients: a new syndrome? [electronic resource] by Plomp, A S Baraitser, M Slaney, S F Winter, R M Producer: 20000211 In: Clinical dysmorphology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	148.	Megalencephaly with dysmyelination, spasticity, ataxia, seizures and distinctive neurophysiological findings in two siblings. [electronic resource] by Harbord, M G Harden, A Harding, B Brett, E M Baraitser, M Producer: 19901204 In: Neuropediatrics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	149.	De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomalies. [electronic resource] by Temple, I K Hurst, J A Hing, S Butler, L Baraitser, M Producer: 19900402 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)
	150.	Partial lipodystrophy syndromes--a further male case. [electronic resource] by Reardon, W Temple, I K Mackinnon, H Leonard, J V Baraitser, M Producer: 19910318 In: Clinical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	151.	Autosomal recessive microcephaly with severe psychomotor retardation. [electronic resource] by Scheffer, I E Baraitser, M Wilson, J Godfrey, C Brett, E M Producer: 19920521 In: Neuropediatrics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	152.	Prenatal treatment of fetal hydrops associated with the hypertelorism-dysphagia syndrome (Opitz-G syndrome). [electronic resource] by Patton, M A Baraitser, M Nickolaides, K Rodeck, C H Gamsu, H Producer: 19860610 In: Prenatal diagnosis vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	153.	The Angelman (Happy Puppet) syndrome: is it autosomal recessive? [electronic resource] by Baraitser, M Patton, M Lam, S T Brett, E M Wilson, J Producer: 19870828 In: Clinical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	154.	The incidence and nature of visual pathway involvement in Friedreich's ataxia. A clinical and visual evoked potential study of 22 patients. [electronic resource] by Carroll, W M Kriss, A Baraitser, M Barrett, G Halliday, A M Producer: 19801027 In: Brain : a journal of neurology vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	155.	The femoral hypoplasia-unusual facies syndrome. [electronic resource] by Burn, J Winter, R M Baraitser, M Hall, C M Fixsen, J Producer: 19850122 In: Journal of medical genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	156.	Nance-Sweeney chondrodysplasia--a further case? [electronic resource] by Rosser, E M Hall, C M Harper, J Lacour, M Baraitser, M Producer: 19961216 In: Clinical dysmorphology vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	157.	Megalocornea, developmental retardation and dysmorphic features: two further patients. [electronic resource] by Gibbs, M L Wilkie, A O Winter, R M Taylor, D Baraitser, M Producer: 19940912 In: Clinical dysmorphology vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	158.	Congenital cutis laxa with retardation of growth and development. [electronic resource] by Patton, M A Tolmie, J Ruthnum, P Bamforth, S Baraitser, M Pembrey, M Producer: 19871208 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)
	159.	The Weissenbacher-Zweymüller, Stickler, and Marshall syndromes: further evidence for their identity. [electronic resource] by Winter, R M Baraitser, M Laurence, K M Donnai, D Hall, C M Producer: 19840107 In: American journal of medical genetics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	160.	DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): elevated plasma and urinary 2-oxoglutarate in three unrelated patients. [electronic resource] by Patton, M A Krywawych, S Winter, R M Brenton, D P Baraitser, M Producer: 19870304 In: American journal of medical genetics vol. 26 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.