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	21.	A mutation in FBN1 disrupts profibrillin processing and results in isolated skeletal features of the Marfan syndrome. [electronic resource] by Milewicz, D M Grossfield, J Cao, S N Kielty, C Covitz, W Jewett, T Producer: 19950605 In: The Journal of clinical investigation vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Fibrillin-1 (FBN1) mutations in patients with thoracic aortic aneurysms. [electronic resource] by Milewicz, D M Michael, K Fisher, N Coselli, J S Markello, T Biddinger, A Producer: 19970102 In: Circulation vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Genetic analysis of structural elastic fiber and collagen genes in familial adolescent idiopathic scoliosis. [electronic resource] by Miller, N H Mims, B Child, A Milewicz, D M Sponseller, P Blanton, S H Producer: 19970127 In: Journal of orthopaedic research : official publication of the Orthopaedic Research Society vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Parental somatic and germ-line mosaicism for a FBN2 mutation and analysis of FBN2 transcript levels in dermal fibroblasts. [electronic resource] by Putnam, E A Park, E S Aalfs, C M Hennekam, R C Milewicz, D M Producer: 19970508 In: American journal of human genetics vol. 60 Availability: No items available. Save to lists Add to cart (remove)
	25.	Characterization of a novel autosomal dominant bleeding disorder in a large kindred from east Texas. [electronic resource] by Kuang, S Q Hasham, S Phillips, M D Wolf, D Wan, Y Thiagarajan, P Milewicz, D M Producer: 20010426 In: Blood vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Delineation of the Marfan phenotype associated with mutations in exons 23-32 of the FBN1 gene. [electronic resource] by Putnam, E A Cho, M Zinn, A B Towbin, J A Byers, P H Milewicz, D M Producer: 19961213 In: American journal of medical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Abnormal fibrillin metabolism in bovine Marfan syndrome. [electronic resource] by Potter, K A Hoffman, Y Sakai, L Y Byers, P H Besser, T E Milewicz, D M Producer: 19930416 In: The American journal of pathology vol. 142 Availability: No items available. Save to lists Add to cart (remove)
	28.	Parental somatic and germ-line mosaicism for a multiexon deletion with unusual endpoints in a type III collagen (COL3A1) allele produces Ehlers-Danlos syndrome type IV in the heterozygous offspring. [electronic resource] by Milewicz, D M Witz, A M Smith, A C Manchester, D K Waldstein, G Byers, P H Producer: 19930723 In: American journal of human genetics vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	29.	Abnormalities in fibrillin 1-containing microfibrils in dermal fibroblast cultures from patients with systemic sclerosis (scleroderma). [electronic resource] by Wallis, D D Tan, F K Kielty, C M Kimball, M D Arnett, F C Milewicz, D M Producer: 20010920 In: Arthritis and rheumatism vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Association of fibrillin 1 single-nucleotide polymorphism haplotypes with systemic sclerosis in Choctaw and Japanese populations. [electronic resource] by Tan, F K Wang, N Kuwana, M Chakraborty, R Bona, C A Milewicz, D M Arnett, F C Producer: 20010503 In: Arthritis and rheumatism vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Reduced penetrance and variable expressivity of familial thoracic aortic aneurysms/dissections. [electronic resource] by Milewicz, D M Chen, H Park, E S Petty, E M Zaghi, H Shashidhar, G Willing, M Patel, V Producer: 19980916 In: The American journal of cardiology vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Association of microsatellite markers near the fibrillin 1 gene on human chromosome 15q with scleroderma in a Native American population. [electronic resource] by Tan, F K Stivers, D N Foster, M W Chakraborty, R Howard, R F Milewicz, D M Arnett, F C Producer: 19981103 In: Arthritis and rheumatism vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	R179H mutation in ACTA2 expanding the phenotype to include prune-belly sequence and skin manifestations. [electronic resource] by Richer, J Milewicz, D M Gow, R de Nanassy, J Maharajh, G Miller, E Oppenheimer, L Weiler, G O'Connor, M Producer: 20120604 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	FBN2 mutation associated with manifestations of Marfan syndrome and congenital contractural arachnodactyly. [electronic resource] by Gupta, P A Wallis, D D Chin, T O Northrup, H Tran-Fadulu, V T Towbin, J A Milewicz, D M Producer: 20040716 In: Journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	Carboxy-terminal conversion of profibrillin to fibrillin at a basic site by PACE/furin-like activity required for incorporation in the matrix. [electronic resource] by Raghunath, M Putnam, E A Ritty, T Hamstra, D Park, E S Tschödrich-Rotter, M Peters, R Rehemtulla, A Milewicz, D M Producer: 19990709 In: Journal of cell science vol. 112 ( Pt 7) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Systemic sclerosis (scleroderma): specific autoantigen genes are selectively overexpressed in scleroderma fibroblasts. [electronic resource] by Zhou, X Tan, F K Xiong, M Milewicz, D M Feghali, C A Fritzler, M J Reveille, J D Arnett, F C Producer: 20011227 In: Journal of immunology (Baltimore, Md. : 1950) vol. 167 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome. [electronic resource] by Adès, L C Morris, L L Power, R G Wilson, M Haan, E A Bateman, J F Milewicz, D M Sillence, D O Producer: 19951103 In: American journal of medical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Clinicopathologic findings in congenital aneurysms of the great vessels. [electronic resource] by Adès, L C Knight, W B Byard, R W Bateman, J F Esquivel, J A Mee, R B Haan, E A Milewicz, D M Producer: 19970321 In: American journal of medical genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	A unique form of hypodontia seen in Vietnamese patients: clinical and molecular analysis. [electronic resource] by Frazier-Bowers, S A Pham, K Y Le, E V Cavender, A C Kapadia, H King, T M Milewicz, D M D'Souza, R N Producer: 20030707 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Comparison of 10 murine models reveals a distinct biomechanical phenotype in thoracic aortic aneurysms. [electronic resource] by Bellini, C Bersi, M R Caulk, A W Ferruzzi, J Milewicz, D M Ramirez, F Rifkin, D B Tellides, G Yanagisawa, H Humphrey, J D Producer: 20180220 In: Journal of the Royal Society, Interface vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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