Your search returned 43 results.

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	1.	Clinical report—health supervision for children with Prader-Willi syndrome. [electronic resource] by McCandless, Shawn E Producer: 20110131 In: Pediatrics vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Answering a Question Older Than Most Pediatricians: What to Do About Duarte Variant Galactosemia. [electronic resource] by McCandless, Shawn E Producer: 20191010 In: Pediatrics vol. 143 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A primer on expanded newborn screening by tandem mass spectrometry. [electronic resource] by McCandless, Shawn E Producer: 20041116 In: Primary care vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Mandatory newborn screening in the United States: History, current status, and existential challenges. [electronic resource] by McCandless, Shawn E Wright, Erica J Producer: 20210818 In: Birth defects research vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Newborn Screening for Lysosomal Storage Disorders: Views of Genetic Healthcare Providers. [electronic resource] by Lisi, Emily C McCandless, Shawn E Producer: 20161213 In: Journal of genetic counseling vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Risk for ingestion of toxic substances in children with Prader-Willi syndrome. [electronic resource] by McCandless, Shawn E Powell, Karen Potter Sandberg, Ulrika Producer: 20130621 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)
	7.	McKusick-Kaufman syndrome: the difficulty of establishing a prenatal diagnosis of an uncommon disorder. [electronic resource] by Slavin, Thomas P McCandless, Shawn E Lazebnik, Noam Producer: 20100616 In: Journal of clinical ultrasound : JCU vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Maculopathy Due to Cobalamin C (cb1C) Disease in an Amish Child. [electronic resource] by Grant, Lorna W McCandless, Shawn E Traboulsi, Elias I Publication details: Journal of pediatric ophthalmology and strabismus Oct 2009 In: Journal of pediatric ophthalmology and strabismus Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	The burden of genetic disease on inpatient care in a children's hospital. [electronic resource] by McCandless, Shawn E Brunger, Jeanne W Cassidy, Suzanne B Producer: 20040301 In: American journal of human genetics vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Inborn Errors of Metabolism with Acidosis: Organic Acidemias and Defects of Pyruvate and Ketone Body Metabolism. [electronic resource] by Schillaci, Lori-Anne P DeBrosse, Suzanne D McCandless, Shawn E Producer: 20181005 In: Pediatric clinics of North America vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	The Global Prader-Willi Syndrome Registry: Development, Launch, and Early Demographics. [electronic resource] by Bohonowych, Jessica Miller, Jennifer McCandless, Shawn E Strong, Theresa V Producer: 20200210 In: Genes vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Sequencing from dried blood spots in infants with "false positive" newborn screen for MCAD deficiency. [electronic resource] by McCandless, Shawn E Chandrasekar, Ram Linard, Sharon Kikano, Sandra Rice, Lorrie Producer: 20130605 In: Molecular genetics and metabolism vol. 108 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome). [electronic resource] by Muenzer, Joseph Gucsavas-Calikoglu, Muge McCandless, Shawn E Schuetz, Thomas J Kimura, Alan Producer: 20070418 In: Molecular genetics and metabolism vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Enzymatic testing sensitivity, variability and practical diagnostic algorithm for pyruvate dehydrogenase complex (PDC) deficiency. [electronic resource] by Shin, Ha Kyung Grahame, George McCandless, Shawn E Kerr, Douglas S Bedoyan, Jirair K Producer: 20180801 In: Molecular genetics and metabolism vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Genomic counseling in the newborn period: experiences and views of genetic counselors. [electronic resource] by Nardini, Monica D Matthews, Anne L McCandless, Shawn E Baumanis, Larisa Goldenberg, Aaron J Producer: 20150330 In: Journal of genetic counseling vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Stopping Parenteral Nutrition for 3 Hours Reduces False Positives in Newborn Screening. [electronic resource] by Tim-Aroon, Thipwimol Harmon, Heidi M Nock, Mary L Viswanathan, Sreekanth K McCandless, Shawn E Producer: 20151020 In: The Journal of pediatrics vol. 167 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Mosaicism for an FMR1 gene deletion in a fragile X female. [electronic resource] by Fan, Hongxin Booker, Jessica K McCandless, Shawn E Shashi, Vandana Fleming, Alison Farber, Rosann A Producer: 20050914 In: American journal of medical genetics. Part A vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	The perils of SNP microarray testing: uncovering unexpected consanguinity. [electronic resource] by Tarini, Beth A Konczal, Laura L Goldenberg, Aaron J Goldman, Edward B McCandless, Shawn E Producer: 20140307 In: Pediatric neurology vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Caregiver priorities for endpoints to evaluate treatments for Prader-Willi syndrome: a best-worst scaling. [electronic resource] by Tsai, Jui-Hua Scheimann, Ann O McCandless, Shawn E Strong, Theresa V Bridges, John F P Producer: 20190409 In: Journal of medical economics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Molecular characterization of a novel, de novo, cryptic interstitial deletion on 19p13.3 in a child with a cutis aplasia and multiple congenital anomalies. [electronic resource] by Al-Kateb, Hussam Hahn, Amanda Gastier-Foster, Julie M Jeng, Linda McCandless, Shawn E Curtis, Christine A Producer: 20110315 In: American journal of medical genetics. Part A vol. 152A 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 43 results.