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	1.	[Maturation of ganglioneuroblastoma to ganglioneuroma: a case report]. [electronic resource] by Niu, D M Chang, T K Liu, S M Hwang, B Producer: 19930603 In: Zhonghua yi xue za zhi = Chinese medical journal; Free China ed vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	2.	Differentiation of hair growth cycle from scalp hair roots for the diagnosis of glucose-6-phosphate dehydrogenase deficiency in neonates. [electronic resource] by Lin, S Y Niu, D M Li, M J Tu, C P Lin, H L Producer: 20010308 In: Journal of inherited metabolic disease vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Chinese achondroplasia is also defined by recurrent G380R mutations of the fibroblast growth factor receptor-3 gene. [electronic resource] by Niu, D M Hsiao, K J Wang, N H Chin, L S Chen, C H Producer: 19960820 In: Human genetics vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Comparison of radioisotopic and ultrasonic scanning in the evaluation of neonatal hypothyroidism. [electronic resource] by Niu, D M Chao, T Tiu, C M Chou, Y H Chu, Y K Hwang, B Producer: 19960522 In: Zhonghua yi xue za zhi = Chinese medical journal; Free China ed vol. 56 Availability: No items available. Save to lists Add to cart (remove)
	5.	Vancomycin resistance due to VanA in an Aerococcus viridans isolate. [electronic resource] by Zhou, W Q Niu, D M Zhang, Z Z Ning, M Z Shen, H Zhang, K Producer: 20150622 In: Indian journal of medical microbiology vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Contribution of genetic factors to neonatal transient hypothyroidism. [electronic resource] by Niu, D-M Lin, C-Y Hwang, B Jap, T-S Liao, C-J Wu, J-Y Producer: 20050127 In: Archives of disease in childhood. Fetal and neonatal edition vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Congenital hypothyroidism with multiple ovarian cysts. [electronic resource] by Chen, C H Tiu, C M Chou, Y H Chen, W Y Hwang, B Niu, D M Producer: 19991117 In: European journal of pediatrics vol. 158 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Diagnosis of congenital hypothyroidism from human anagen scalp hair by infrared microspectroscopy. [electronic resource] by Lin, S Y Niu, D M Tu, C P Lin, H L Li, M J Cheng, Y D Producer: 20020418 In: Ultrastructural pathology vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Contributions of bone maturation measurements to the differential diagnosis of neonatal transient hypothyroidism versus dyshormonogenetic congenital hypothyroidism. [electronic resource] by Niu, D M Hwang, B Tiu, C M Tsai, L P Yen, J L Lee, N C Lin, C Y Producer: 20050104 In: Acta paediatrica (Oslo, Norway : 1992) vol. 93 Availability: No items available. Save to lists Add to cart (remove)
	10.	A pilot study of neonatal screening by electrospray ionization tandem mass spectrometry in Taiwan. [electronic resource] by Lin, W D Wu, J Y Lai, C C Tsai, F J Tsai, C H Lin, S P Niu, D M Producer: 20011004 In: Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	11.	DiGeorge syndrome with microdeletion of chromosome 22q11.2: report of one case. [electronic resource] by Wang, J L Chen, S J Chung, M Y Niu, D M Lin, C Y Hwang, B T Lu, J H Producer: 19971231 In: Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	12.	Brain MR Imaging Findings of Cardiac-Type Fabry Disease with an IVS4+919G>A Mutation. [electronic resource] by Lee, H-J Hung, S-C Hsu, T-R Ko, S-C Chui-Mei, T Huang, C-C Niu, D-M Lin, C-P Producer: 20171120 In: AJNR. American journal of neuroradiology vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	R1193Q of SCN5A, a Brugada and long QT mutation, is a common polymorphism in Han Chinese. [electronic resource] by Hwang, H W Chen, J J Lin, Y J Shieh, R C Lee, M T Hung, S I Wu, J Y Chen, Y T Niu, D M Hwang, B T Producer: 20060420 In: Journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	A whole genome methylation analysis of systemic lupus erythematosus: hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity. [electronic resource] by Lin, S-Y Hsieh, S-C Lin, Y-C Lee, C-N Tsai, M-H Lai, L-C Chuang, E Y Chen, P-C Hung, C-C Chen, L-Y Hsieh, W S Niu, D-M Su, Y-N Ho, H-N Producer: 20120820 In: Genes and immunity vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)