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	1.	Pitfalls of diagnostic screening for inborn errors of metabolism. [electronic resource] by Rouse, B M Producer: 19690807 In: Texas medicine vol. 65 Availability: No items available. Save to lists Add to cart (remove)
	2.	Phenylalanine deficiency syndrome. [electronic resource] by Rouse, B M Producer: 19661018 In: The Journal of pediatrics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mesodermal origin of axial dysraphism. [electronic resource] by Ferguson, J W Rouse, B M Lockhart, L Producer: 19831008 In: The Journal of pediatrics vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Ocular, cerebral and cutaneous malformations: confirmation of an association. [electronic resource] by Ferguson, J W Hutchison, H T Rouse, B M Producer: 19840709 In: Clinical genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	CYTOGENETIC STUDIES. DIAGNOSTIC TOOL IN CLINICAL MEDICINE. [electronic resource] by ROUSE, B M LOCKHART, L H HAGGARD, M E Producer: 19961201 In: Texas state journal of medicine vol. 60 Availability: No items available. Save to lists Add to cart (remove)
	6.	Proximal duplications of chromosome 15: clinical dilemmas. [electronic resource] by Hood, O J Rouse, B M Lockhart, L H Bodensteiner, J B Producer: 19860602 In: Clinical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	An enzymatic assay of plasma phenylalanine and tyrosine for the detection and management of phenylketonuria. [electronic resource] by Shen, R S Richardson, C J Rouse, B M Abell, C W Producer: 19820212 In: Biochemical medicine vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A complex chromosomal rearrangement and congenital anomalies in the progeny of a mother treated for childhood leukemia. [electronic resource] by McCombs, J L Daeschner, C W Lockhart, L H Rouse, B M Heath, D V Producer: 19910118 In: Cancer genetics and cytogenetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Clinical nutrition applications of space food technology. [electronic resource] by Heidelbaugh, N D Smith, M C Rambaut, P C Lutwak, L Huber, C S Stadler, C R Rouse, B M Producer: 19730510 In: Journal of the American Dietetic Association vol. 62 Availability: No items available. Save to lists Add to cart (remove)
	10.	Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative Study. [electronic resource] by Guldberg, P Levy, H L Hanley, W B Koch, R Matalon, R Rouse, B M Trefz, F de la Cruz, F Henriksen, K F Güttler, F Producer: 19960801 In: American journal of human genetics vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	11.	Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: report from the Maternal Phenylketonuria Collaborative Study. [electronic resource] by Güttler, F Azen, C Guldberg, P Romstad, A Hanley, W B Levy, H L Matalon, R Rouse, B M Trefz, F de la Cruz, F Koch, R Producer: 19990819 In: Pediatrics vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative Study. [electronic resource] by Levy, H L Guldberg, P Güttler, F Hanley, W B Matalon, R Rouse, B M Trefz, F Azen, C Allred, E N de la Cruz, F Koch, R Producer: 20010628 In: Pediatric research vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)