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L P Tsai

Showing results (1-10 of 9) with videos related to

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Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|August 6, 2000
EEG--a valuable tool in early diagnosis of Angelman syndromeC C Sue, P L Kuo, L P Tsai
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|October 6, 2000
Bilateral ulnar hemimelia in Brachmann-de Lange syndrome: report of one caseY C Chao, L P Tsai, Y W Chang, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|January 1, 1996
Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutationL P Tsai, W C Sue, W L Hwu, et al.
Clinical Genetics|May 23, 2009
A novel microdeletion at chromosome 2q31.1-31.2 in a three-generation family presenting duplication of great toes with clinodactylyL-P Tsai, H-M Liao, Y-J Chen, et al.
Human Genetics|February 1, 1996
Arylsulfatase A pseudodeficiency in ChineseW L Hwu, L P Tsai, W C Wang, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 27, 2004
Contributions of bone maturation measurements to the differential diagnosis of neonatal transient hypothyroidism versus dyshormonogenetic congenital hypothyroidismD M Niu, B Hwang, C M Tiu, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|March 30, 2001
An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndromeC C Tzeng, S J Lin, Y J Chen, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000
An R248C mutation of FGFR3 leading to thanatophoric dysplasia type IF J Tsai, L P Tsai, S P Lin, et al.
Clinical Genetics|February 1, 2017
A 15-year-long Southern blotting analysis of FMR1 to detect female carriers and for prenatal diagnosis of fragile X syndrome in TaiwanC-C Tzeng, L-P Tsai, Y-K Chang, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|August 6, 2000
EEG--a valuable tool in early diagnosis of Angelman syndromeC C Sue, P L Kuo, L P Tsai
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|October 6, 2000
Bilateral ulnar hemimelia in Brachmann-de Lange syndrome: report of one caseY C Chao, L P Tsai, Y W Chang, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|January 1, 1996
Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutationL P Tsai, W C Sue, W L Hwu, et al.
Clinical Genetics|May 23, 2009
A novel microdeletion at chromosome 2q31.1-31.2 in a three-generation family presenting duplication of great toes with clinodactylyL-P Tsai, H-M Liao, Y-J Chen, et al.
Human Genetics|February 1, 1996
Arylsulfatase A pseudodeficiency in ChineseW L Hwu, L P Tsai, W C Wang, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 27, 2004
Contributions of bone maturation measurements to the differential diagnosis of neonatal transient hypothyroidism versus dyshormonogenetic congenital hypothyroidismD M Niu, B Hwang, C M Tiu, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|March 30, 2001
An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndromeC C Tzeng, S J Lin, Y J Chen, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000
An R248C mutation of FGFR3 leading to thanatophoric dysplasia type IF J Tsai, L P Tsai, S P Lin, et al.
Clinical Genetics|February 1, 2017
A 15-year-long Southern blotting analysis of FMR1 to detect female carriers and for prenatal diagnosis of fragile X syndrome in TaiwanC-C Tzeng, L-P Tsai, Y-K Chang, et al.
Pageof 1