Your search returned 22 results.

Results
	1.	Turner's syndrome: updating on diagnosis and therapy. [electronic resource] by De Paepe, A Matton, M Producer: 19860220 In: Progress in clinical and biological research vol. 200 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Genetic aspects of melanoma]. [electronic resource] by Matton, M T Verschraegen-Spae, M R Producer: 19750503 In: Acta chirurgica Belgica vol. 73 Availability: No items available. Save to lists Add to cart (remove)
	3.	THE MECHANISM OF DEATH FROM QUINIDINE AND A METHOD OF RESUSCITATION; AN EXPERIMENTAL STUDY. [electronic resource] by Gordon, B Matton, M Levine, S A Producer: 20060531 In: The Journal of clinical investigation vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Genetic aspects of childhood tumours. [electronic resource] by Francois, J De Bie, S Matton, M Producer: 19760706 In: Acta geneticae medicae et gemellologiae vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Familial dermatoglyphic analysis in syndactyly type I. [electronic resource] by Matton, M De Bie, S Anseeuw, A Producer: 19820212 In: The Journal of hand surgery vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Pulse wave velocity recordings in a family with ecchymotic Ehlers-Danlos syndrome. [electronic resource] by François, B De Paepe, A Matton, M T Clement, D Producer: 19860917 In: International angiology : a journal of the International Union of Angiology vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	7.	[Heredity of congenital deficiencies in color vision]. [electronic resource] by François, J De Bie, S Verriest, G Matton, M T Producer: 19740429 In: Acta geneticae medicae et gemellologiae vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	[Intermittent and persistent vaginal discharge following amniocentesis]. [electronic resource] by Verschraegen-Spae, M R Van den Wijngaert, J Matton, M T Producer: 19810421 In: Journal de genetique humaine vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	9.	[The Ehlers-Danlos and Marfan syndromes in young children]. [electronic resource] by De Paepe, A Van den Bossche, H Mortier, G Matton, M Producer: 19881013 In: Journal de genetique humaine vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	10.	Unusual familial manifestation of Ehlers-Danlos syndrome. [electronic resource] by Matton, M T De Paepe, A De Keyser, F François, B Producer: 19830415 In: Progress in clinical and biological research vol. 104 Availability: No items available. Save to lists Add to cart (remove)
	11.	Long-term Preservation of Donor Tissue for Corneal Grafting: Correlation of Results from Tissue Cultures with Those from Experimental Graftings. [electronic resource] by Stocker, F W Matton, M T Eiring, A Georgiade, R Georgiade, N Producer: 20060601 In: Transactions of the American Ophthalmological Society vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	12.	Genesis and genetics of retinoblastoma. [electronic resource] by François, J Matton, M T De Bie, S Tanaka, Y Vandenbulcke, D Producer: 19751108 In: Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Familial congenital esophageal atresia. Personal case report and review of the literature. [electronic resource] by Van Staey, M De Bie, S Matton, M T De Roose, J Producer: 19840530 In: Human genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Longterm preservation of donor tissue for corneal grafting; correlation of results from tissue cultures with those from experimental graftings. [electronic resource] by STOCKER, F W MATTON, M T EIRING, A GEORGIADE, R GEORGIADE, N Producer: 19981101 In: American journal of ophthalmology vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	15.	Obstetrical problems in patients with Ehlers-Danlos syndrome type IV; a case report. [electronic resource] by De Paepe, A Thaler, B Van Gijsegem, M Van Hoecke, D Matton, M Producer: 19900110 In: European journal of obstetrics, gynecology, and reproductive biology vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Trisomy 3 mosaicism in a patient with Bartter syndrome. [electronic resource] by De Keyser, F Matthys, E De Paepe, A Verschraegen-Spae, M R Matton, M Producer: 19880808 In: Journal of medical genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Dominant optic nerve atrophy with progressive hearing loss and chronic progressive external ophthalmoplegia (CPEO). [electronic resource] by Meire, F De Laey, J J de Bie, S van Staey, M Matton, M T Producer: 19851219 In: Ophthalmic paediatrics and genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Dermatoglyphic analysis of primary and secondary cleft palate patients. [electronic resource] by De Bie, S Hayashi, M Matton, M T Matton, G Vrijdagh, S Lejour, M Buts, R Castermans, A Producer: 19770922 In: The Cleft palate journal vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	19.	Linkage of a polymorphic marker for the type III collagen gene (COL3A1) to atypical autosomal dominant Ehlers-Danlos syndrome type IV in a large Belgian pedigree. [electronic resource] by Nicholls, A C De Paepe, A Narcisi, P Dalgleish, R De Keyser, F Matton, M Pope, F M Producer: 19880418 In: Human genetics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Ehlers-Danlos syndrome type I: a clinical and ultrastructural study of a family with reduced amounts of collagen type III. [electronic resource] by De Paepe, A Nicholls, A Narcisi, P De Keyser, F Quatacker, J Van Staey, M Matton, M Pope, F M Producer: 19871120 In: The British journal of dermatology vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search

Availability

Authors

Topics

Languages

Your search returned 22 results.