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	1.	Identical twins with Cohen syndrome. [electronic resource] by North, K N Fulton, A B Whiteman, D A Producer: 19951120 In: American journal of medical genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Treacher Collins syndrome: phenotypic variability in a family including an infant with arhinia and uveal colobomas. [electronic resource] by Hansen, M Lucarelli, M J Whiteman, D A Mulliken, J B Producer: 19961009 In: American journal of medical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Cerebrovascular complications in Ehlers-Danlos syndrome type IV. [electronic resource] by North, K N Whiteman, D A Pepin, M G Byers, P H Producer: 19960123 In: Annals of neurology vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Brief clinical report: a 46,XY phenotypic female with Smith-Lemli-Opitz syndrome. [electronic resource] by Lachman, M F Wright, Y Whiteman, D A Herson, V Greenstein, R M Producer: 19910522 In: Clinical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Folate deficiency and acute intermittent porphyria in a 12-year-old boy. [electronic resource] by DiMario, F J Quinn, J J Zalneraitis, E L Whiteman, D A Russman, B S Producer: 19930809 In: Neurology vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	CHARGE association in a child with de novo inverted duplication (14)(q22-->q24.3). [electronic resource] by North, K N Wu, B L Cao, B N Whiteman, D A Korf, B R 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)
	7.	Chromosome 7p--syndrome: craniosynostosis with preservation of region 7p2. [electronic resource] by Aughton, D J Cassidy, S B Whiteman, D A Delach, J A Guttmacher, A E Producer: 19920115 In: American journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	The relationship between anti-idursulfase antibody status and safety and efficacy outcomes in attenuated mucopolysaccharidosis II patients aged 5 years and older treated with intravenous idursulfase. [electronic resource] by Barbier, A J Bielefeld, B Whiteman, D A H Natarajan, M Pano, A Amato, D A Producer: 20140508 In: Molecular genetics and metabolism vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	The human ribosomal RNA genes: structure and organization of the complete repeating unit. [electronic resource] by Sylvester, J E Whiteman, D A Podolsky, R Pozsgay, J M Respess, J Schmickel, R D Producer: 19860917 In: Human genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Hypoglycinaemia and psychomotor delay in a child with xeroderma pigmentosum. [electronic resource] by Quackenbush, E J Kraemer, K H Gahl, W A Schirch, V Whiteman, D A Levine, K Levy, H L Producer: 20000124 In: Journal of inherited metabolic disease vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Mucolipidosis type IV: clinical manifestations and natural history. [electronic resource] by Chitayat, D Meunier, C M Hodgkinson, K A Silver, K Flanders, M Anderson, I J Little, J M Whiteman, D A Carpenter, S Producer: 19920326 In: American journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Evaluation of impact of anti-idursulfase antibodies during long-term idursulfase enzyme replacement therapy in mucopolysaccharidosis II patients. [electronic resource] by Giugliani, R Harmatz, P Jones, S A Mendelsohn, N J Vellodi, A Qiu, Y Hendriksz, C J Vijayaraghavan, S Whiteman, D A H Pano, A Publication details: Molecular genetics and metabolism reports Sep 2017 In: Molecular genetics and metabolism reports vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted. [electronic resource] by Weksberg, R Teshima, I Williams, B R Greenberg, C R Pueschel, S M Chernos, J E Fowlow, S B Hoyme, E Anderson, I J Whiteman, D A Producer: 19930727 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)