Your search returned 45 results.

Results
	1.	Vici syndrome: a rare autosomal recessive syndrome with brain anomalies, cardiomyopathy, and severe intellectual disability. [electronic resource] by Rogers, R Curtis Aufmuth, Bridgette Monesson, Stephanie Producer: 20121024 In: Case reports in genetics vol. 2011 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Malformations among the X-linked intellectual disability syndromes. [electronic resource] by Stevenson, Roger E Schwartz, Charles E Rogers, R Curtis Producer: 20140731 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Congenital livedo reticularis and recurrent strokes in two unrelated young children. [electronic resource] by Mathias, Gretchen Cowley, Ron Morales, Augusto Rogers, R Curtis Producer: 20061019 In: Clinical pediatrics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Brittle cornea syndrome: a case report and comparison with Ehlers Danlos syndrome. [electronic resource] by Ramappa, Muralidhar Wilson, M Edward Rogers, R Curtis Trivedi, Rupal H Producer: 20150625 In: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Reply: To PMID 25266838. [electronic resource] by Ramappa, Muralidhar Wilson, M Edward Trivedi, Rupal H Rogers, R Curtis Producer: 20150626 In: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Behavioral features in young adults with FG syndrome (Opitz-Kaveggia syndrome). [electronic resource] by Graham, John M Clark, Robin D Moeschler, John B Rogers, R Curtis Producer: 20110218 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 154C Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitalia. [electronic resource] by Bhat, Shambhu S Rogers, R Curtis Holden, Kenton R Srivastava, Anand K Producer: 20050928 In: American journal of medical genetics. Part A vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Seizures and X-linked intellectual disability. [electronic resource] by Stevenson, Roger E Holden, Kenton R Rogers, R Curtis Schwartz, Charles E Producer: 20121017 In: European journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Letter to the editor regarding Disciglio et al.: interstitial 22q13 deletions not involving SHANK3 gene: a new contiguous gene syndrome. [electronic resource] by Phelan, Katy Boccuto, Luigi Rogers, R Curtis Sarasua, Sara M McDermid, Heather E Producer: 20150821 In: American journal of medical genetics. Part A vol. 167 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Velocardiofacial syndrome in an unexplained XX male. [electronic resource] by Phelan, Mary C Rogers, R Curtis Crawford, Eric C Brown, Laura G Page, David C Producer: 20030530 In: American journal of medical genetics. Part A vol. 116A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Finding new etiologies of mental retardation and hypotonia: X marks the spot. [electronic resource] by Rogers, R Curtis Stevenson, Roger E Simensen, Richard J Holden, Kenton R Schwartz, Charles E Producer: 20080225 In: Developmental medicine and child neurology vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Long-term observation of a patient with dominant omodysplasia. [electronic resource] by Gordon, Barbara L Champaigne, Neena L Rogers, R Curtis Frias, Jaime L Leroy, Jules G Producer: 20150819 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Growth in Phelan-McDermid syndrome. [electronic resource] by Rollins, Jonathan D Sarasua, Sara M Phelan, Katy DuPont, Barbara R Rogers, R Curtis Collins, Julianne S Producer: 20120209 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Do patients with Down syndrome develop appendicitis? [electronic resource] by Lewis, M Elizabeth N Gauderer, Michael W L Blackhurst, Dawn W Rogers, R Curtis Cornett, Wendy R Producer: 20110627 In: Journal of pediatric surgery vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Confirmation of spondylo-epi-metaphyseal dysplasia with joint laxity, EXOC6B type. [electronic resource] by Campos-Xavier, Belinda Rogers, R Curtis Niel-Bütschi, Florence Ferreira, Catarina Unger, Sheila Spranger, Jürgen Superti-Furga, Andrea Producer: 20191029 In: American journal of medical genetics. Part A vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype. [electronic resource] by Holden, Kenton R Zuñiga, Oscar F May, Melanie M Su, Humberto Molinero, Marco R Rogers, R Curtis Schwartz, Charles E Producer: 20060224 In: Journal of child neurology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	A previously unreported mutation in a Currarino syndrome kindred. [electronic resource] by Wang, Raymond Y Jones, Julie R Chen, Steve Rogers, R Curtis Friez, Michael J Schwartz, Charles E Graham, John M Producer: 20061024 In: American journal of medical genetics. Part A vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	The intellectual disabilities evaluation and advice system (IDEAS): outcome of the first 55 cases. [electronic resource] by Hunter, Alasdair G W Graham, John M Neri, Giovanni Rogers, R Curtis Stevenson, Roger E Turner, Gillian Friez, Michael J Producer: 20150820 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Novel human pathological mutations. Gene symbol: JARID1C. Disease: mental retardation, X-linked. [electronic resource] by Abidi, Fatima Holloway, Lynda Moore, Cynthia A Weaver, David D Simensen, Richard J Stevenson, Roger E Rogers, R Curtis Schwartz, Charles E Producer: 20090414 In: Human genetics vol. 125 Availability: No items available. Save to lists Add to cart (remove)
	20.	Novel human pathological mutations. Gene symbol: JARID1C. Disease: mental retardation, X-linked. [electronic resource] by Abidi, Fatima Holloway, Lynda Moore, Cynthia A Weaver, David D Simensen, Richard J Stevenson, Roger E Rogers, R Curtis Schwartz, Charles E Producer: 20090414 In: Human genetics vol. 125 Availability: No items available. Save to lists Add to cart (remove)

1
2
3
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 45 results.