• 17936 Citations
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1991 …2019
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Research Output 1991 2019

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Letter
2016
1 Citation (Scopus)

Genetic screening of the makorin ring finger 3 gene in girls with idiopathic central precocious puberty

Lin, W. D., Wang, C. H. & Tsai, F-J., Mar 1 2016, In : Clinical Chemistry and Laboratory Medicine. 54, 3, p. e93-e96

Research output: Contribution to journalLetter

2014
1 Citation (Scopus)

A novel one-base insertion mutation in the retinitis pigmentosa 2 gene in a large X-linked Taiwanese family

Lin, W. D., Wang, C. H., Chou, I. C. & Tsai, F-J., Mar 1 2014, In : Acta Ophthalmologica. 92, 2

Research output: Contribution to journalLetter

X-Linked Genetic Diseases
Eye Proteins
Molecular Sequence Data
Intracellular Signaling Peptides and Proteins
Frameshift Mutation
4 Citations (Scopus)

Prominent vacuolation of the eyelid levator muscle in an early-treated child with infantile-onset Pompe disease

Chien, Y. H., Lee, N. C., Tsai, Y. J., Thurberg, B. L., Tsai, F-J. & Hwu, W. L., Jan 1 2014, In : Muscle and Nerve. 50, 2, p. 301-302 2 p.

Research output: Contribution to journalLetter

Oculomotor Muscles
Glycogen Storage Disease Type II
Eyelids
Vacuoles
Muscles
2011

Congenital tracheal stenosis in a boy with the 22q13.3 deletion syndrome

Chen, C. P., Lin, S. P., Tsai, F-J., Chern, S. R., Wu, P. C., Lee, C. C., Lee, M. S., Chen, Y. T. & Wang, W., 2011, In : Genetic Counseling. 22, 1, p. 79-83 5 p.

Research output: Contribution to journalLetter

2 Citations (Scopus)

Genetic and clinical profiles of spondylocostal dysostosis patients in Taiwan

Wang, C. H., Lin, W. D., Bau, D-T., Chou, I. C. & Tsai, F-J., Dec 1 2011, In : American Journal of Medical Genetics, Part A. 155, 12, p. 3132-3135 4 p.

Research output: Contribution to journalLetter

Intracellular Signaling Peptides and Proteins
Multiple Abnormalities
Basic Helix-Loop-Helix Transcription Factors
Glycosyltransferases
Diaphragmatic Hernia
1 Citation (Scopus)

Mosaic ring chromosome 4 in a child with mild dysmorphisms, congenital heart defects and developmental delay

Chen, C. P., Lin, S. P., Su, Y. N., Chern, S. R., Tsai, F-J., Wu, P. C., Lee, C. C. & Wang, W., Oct 20 2011, In : Genetic Counseling. 22, 3, p. 321-326 6 p.

Research output: Contribution to journalLetter

Reply

Lin, J. M., Tsai, Y. Y. & Tsai, F-J., Sep 2011, In : Retina. 31, 8, p. 1743-1744 2 p.

Research output: Contribution to journalLetter

5 Citations (Scopus)

Self-injurious behavior associated with trisomy 9p (9p13.1→p24.3)

Chen, C. P., Lin, S. P., Su, Y. N., Chern, S. R., Tsai, F-J., Chen, W. L. & Wang, W., Oct 20 2011, In : Genetic Counseling. 22, 3, p. 327-331 5 p.

Research output: Contribution to journalLetter

2010
11 Citations (Scopus)

Abnormally Flat Facial Profile on Two- and Three-dimensional Ultrasound and Array Comparative Genomic Hybridization for the Diagnosis of Pallister-Killian Syndrome

Chen, C. P., Su, Y. N., Hsu, C. Y., Tsai, F-J., Chien, S. C., Chern, S. R., Lee, M. S., Wu, P. C., Chen, H. E. C. & Wang, W., Mar 1 2010, In : Taiwanese Journal of Obstetrics and Gynecology. 49, 1, p. 124-128 5 p.

Research output: Contribution to journalLetter

Craniofacial Abnormalities
Prenatal Ultrasonography
Multiple Abnormalities
Chromosomes, Human, Pair 12
Mosaicism
6 Citations (Scopus)

A new familial insertion, ins(18;9)(q12.2;q33.1q31.1) with a 9q31.1-9q33.1 deletion in a girl with a cleft lip and palate

Chien, S. C., Li, Y. C., Li, N. H., Wu, J. Y., Hsu, P. C., Shi, S. L., Tsai, F-J. & Lin, C. C., Jan 1 2010, In : American Journal of Medical Genetics, Part A. 152, 7, p. 1862-1867 6 p.

Research output: Contribution to journalLetter

Chromosome Banding
Chromosomes, Human, Pair 18
Bacterial Artificial Chromosomes
Chromosome Deletion
Chromosomes, Human, Pair 9
3 Citations (Scopus)

Apert syndrome associated with upper airway obstruction and gastroesophageal reflux inducing polyhydramnios in the third trimester

Chen, C. P., Lin, S. P., Su, Y. N., Chen, C. Y., Tsai, F-J., Liu, Y. P., Chern, S. R., Wu, P. C., Chen, H. E. C. & Wang, W., Jun 1 2010, In : Taiwanese Journal of Obstetrics and Gynecology. 49, 2, p. 231-234 4 p.

Research output: Contribution to journalLetter

Acrocephalosyndactylia
Newborn Respiratory Distress Syndrome
Polyhydramnios
Third Pregnancy Trimester
Airway Obstruction
5 Citations (Scopus)

Deletion 2q37.3→qter and duplication 15q24.3→qter characterized by array CGH in a girl with epilepsy and dysmorphic features

Chen, C. P., Lin, S. P., Chern, S. R., Tsai, F-J., Wu, P. C., Lee, C. C., Chen, L. F., Lee, M. S. & Wang, W., 2010, In : Genetic Counseling. 21, 2, p. 263-267 5 p.

Research output: Contribution to journalLetter

Multiple Abnormalities
Chromosomes, Human, Pair 15
Chromosome Deletion
Gene Duplication
Comparative Genomic Hybridization
1 Citation (Scopus)

Detection of Balanced Homologous Acrocentric Rearrangement REA(14Q14Q) and Low-Grade X-Chromosome Mosaicism in a Couple With Repeated Pregnancy Losses

Chen, C. P., Chern, S. R., Wu, C. H., Tsai, F-J., Wu, P. C. & Wang, W., Jun 1 2010, In : Taiwanese Journal of Obstetrics and Gynecology. 49, 2, p. 239-242 4 p.

Research output: Contribution to journalLetter

Sex Chromosome Aberrations
Chromosomes, Human, 13-15
Chromosomes, Human, X
Habitual Abortion
Genetic Translocation
2 Citations (Scopus)

Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with joubert syndrome

Chen, C. P., Su, Y. N., Huang, J. K., Liu, Y. P., Tsai, F-J., Yang, C. K., Huang, J. P., Chen, C. Y., Wu, P. C. & Wang, W., Jun 1 2010, In : Taiwanese Journal of Obstetrics and Gynecology. 49, 2, p. 243-246 4 p.

Research output: Contribution to journalLetter

Nervous System Malformations
Polydactyly
Toes
Fingers
Central Nervous System
4 Citations (Scopus)

Mosaic tetrasomy 12P with discrepancy between fetal tissues and extraembryonic tissues: Molecular analysis and possible mechanism of formation

Chen, C. P., Su, Y. N., Chern, S. R., Tsai, F-J., Wu, P. C., Chen, H. E. C., Chiang, S. S. & Wang, W., Jun 1 2010, In : Taiwanese Journal of Obstetrics and Gynecology. 49, 2, p. 235-238 4 p.

Research output: Contribution to journalLetter

Chromosome Disorders
Isochromosomes
Chorionic Villi Sampling
Chromosomes, Human, Pair 12
Karyotyping
6 Citations (Scopus)

Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 21

Chen, C. P., Lin, C. C., Ko, T. M., Tsai, F-J., Chern, S. R., Lee, C. C., Chen, Y. T., Wu, P. C. & Wang, W., Sep 1 2010, In : Taiwanese Journal of Obstetrics and Gynecology. 49, 3, p. 377-380 4 p.

Research output: Contribution to journalLetter

Nucleic Acid Amplification Techniques
Chromosomes, Human, Pair 21
Amniocentesis
Gene Dosage
Prenatal Diagnosis
4 Citations (Scopus)

Prenatal Diagnosis of a 4.9-Mb Deletion of 10q11.21 → q11.23 by Array Comparative Genomic Hybridization

Chen, C. P., Su, Y. N., Chern, S. R., Tsai, F-J., Hsu, C. Y., Lee, C. C. & Wang, W., Mar 1 2010, In : Taiwanese Journal of Obstetrics and Gynecology. 49, 1, p. 117-119 3 p.

Research output: Contribution to journalLetter

Chromosomes, Human, Pair 10
Chromosome Deletion
Comparative Genomic Hybridization
Amniocentesis
Induced Abortion
4 Citations (Scopus)

Prenatal Diagnosis of Persistent Cloaca With Hydrometrocolpos and Ascites by Magnetic Resonance Imaging in One Fetus of a Dizygotic Twin Pregnancy

Chen, C. P., Liu, Y. P., Chang, T. Y., Tsai, F-J., Chen, C. Y., Wu, P. C., Chen, T. H. T. & Wang, W., Sep 1 2010, In : Taiwanese Journal of Obstetrics and Gynecology. 49, 3, p. 385-386 2 p.

Research output: Contribution to journalLetter

Hydrocolpos
Uterine Diseases
Prenatal Ultrasonography
Cloaca
Fetal Diseases
6 Citations (Scopus)

Prenatal Diagnosis of Rhabdomyomas and Cerebral Tuberous Sclerosis by Magnetic Resonance Imaging in One Fetus of a Dizygotic Twin Pregnancy Associated With a Frameshift Mutation in the TSC2 Gene

Chen, C. P., Su, Y. N., Chang, T. Y., Liu, Y. P., Tsai, F-J., Chen, M. R., Hwang, J. K., Chen, T. H. T. & Wang, W., Sep 1 2010, In : Taiwanese Journal of Obstetrics and Gynecology. 49, 3, p. 387-389 3 p.

Research output: Contribution to journalLetter

Rhabdomyoma
Fetal Diseases
Tumor Suppressor Proteins
Dizygotic Twins
Frameshift Mutation
1 Citation (Scopus)

Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q

Chen, C. P., Tsai, F-J., Lee, C. C., Chen, W. L., Pan, C. W., Wu, P. C. & Wang, W., Oct 14 2010, In : Genetic Counseling. 21, 3, p. 353-357 5 p.

Research output: Contribution to journalLetter

Chromosome Banding
Satellite DNA
Nucleolus Organizer Region
Chromosomes, Human, Pair 21
Karyotyping
9 Citations (Scopus)
Amnion
Comparative Genomic Hybridization
Amniocentesis
Third Pregnancy Trimester
Second Pregnancy Trimester
2 Citations (Scopus)

Reduction in imiglucerase dosage causes immediate rise of chitotriosidase activity in patients with Gaucher disease

Chien, Y. H., Lee, N. C., Tsai, F-J., Chao, M. C. & Hwu, W. L., Sep 1 2010, In : Molecular Genetics and Metabolism. 101, 1, p. 90-91 2 p.

Research output: Contribution to journalLetter

Glucosylceramidase
Hexosaminidases
chitotriosidase
imiglucerase

Reply to Guggenheim et al

Lin, H. J., Wan, L., Tsai, Y., Chen, W. C., Tsai, S. W. & Tsai, F-J., Jan 1 2010, In : Eye. 24, 8, 1 p.

Research output: Contribution to journalLetter

11 Citations (Scopus)

Second-trimester Molecular Prenatal Diagnosis of Sporadic Apert Syndrome Following Sonographic Findings of Mild Ventriculomegaly and Clenched Hands Mimicking Trisomy 18

Chen, C. P., Su, Y. N., Hsu, C. Y., Ling, P. Y., Tsai, F-J., Chern, S. R., Wu, P. C., Chen, H. E. C. & Wang, W., Mar 1 2010, In : Taiwanese Journal of Obstetrics and Gynecology. 49, 1, p. 129-132 4 p.

Research output: Contribution to journalLetter

Receptor, Fibroblast Growth Factor, Type 2
Craniofacial Abnormalities
Acrocephalosyndactylia
Nucleic Acid Hybridization
Cerebral Ventricles
2009
3 Citations (Scopus)

Prenatal Diagnosis and Molecular Analysis of Triploidy in a Fetus With Intrauterine Growth Restriction, Relative Macrocephaly and Holoprosencephaly

Chen, C. P., Chern, S. R., Tsai, F-J., Hsu, C. Y., Ko, K. & Wang, W., Sep 1 2009, In : Taiwanese Journal of Obstetrics and Gynecology. 48, 3, p. 323-326 4 p.

Research output: Contribution to journalLetter

Prenatal Ultrasonography
Megalencephaly
Holoprosencephaly
Triploidy
Polyploidy
6 Citations (Scopus)

Prenatal Diagnosis and Molecular Analysis of Trisomy 13 Mosaicism

Chen, C. P., Chern, S. R., Tsai, F-J., Lin, H. H., Pan, C. W. & Wang, W., Sep 1 2009, In : Taiwanese Journal of Obstetrics and Gynecology. 48, 3, p. 321-322 2 p.

Research output: Contribution to journalLetter

Therapeutic Abortion
Chromosomes, Human, Pair 13
Mosaicism
Trisomy
Genetic Testing
3 Citations (Scopus)

Prenatal diagnosis of 46,XX, der(13;21)(Q10;Q1 0),+21 and transient abnormal myelopoiesis in a fetus with hepatosplenomegaly and spontaneous resolution of fetal ascites

Chen, C. P., Tsai, F-J., Chern, S. R., Chang, T. Y., Hsu, C. Y., Lin, H. H. & Wang, W., Jan 1 2009, In : Taiwanese Journal of Obstetrics and Gynecology. 48, 1, p. 84-87 4 p.

Research output: Contribution to journalLetter

Mixed Gonadal Dysgenesis
Cordocentesis
Prenatal Ultrasonography
Karyotyping
Fetal Death
4 Citations (Scopus)

Prenatal diagnosis of partial trisomy 14q (14q31.1→qter) and partial monosomy 5p (5p13.2→pter) associated with polyhydramnios, short limbs, micropenis and brain malformations

Chen, C. P., Chern, S. R., Tsai, F-J., Lee, C. C., Chen, L. F. & Wang, W., 2009, In : Genetic Counseling. 20, 3, p. 281-288 8 p.

Research output: Contribution to journalLetter

Eugenic Abortion
Prenatal Ultrasonography
Ectromelia
Multiple Abnormalities
Polyhydramnios
6 Citations (Scopus)

Prenatal Magnetic Resonance Imaging, Ultrasound Imaging Findings and Genetic Analysis of Concomitant Rhabdomyomas and Cerebral Tuberous Sclerosis

Chen, C. P., Su, Y. N., Chang, T. Y., Liu, Y. P., Tsai, F-J., Hwang, J. K. & Wang, W., Sep 1 2009, In : Taiwanese Journal of Obstetrics and Gynecology. 48, 3, p. 327-331 5 p.

Research output: Contribution to journalLetter

Echoencephalography
Rhabdomyoma
Prenatal Ultrasonography
Heart Neoplasms
Tuberous Sclerosis
2008

Occipital encephalocele associated with iniencephaly mimicking an unilateral nuchal tumor on prenatal ultrasound

Chen, C. P., Hwu, Y. M., Tsai, F-J. & Wang, W., 2008, In : Genetic Counseling. 19, 1, p. 101-103 3 p.

Research output: Contribution to journalLetter

Fetal Diseases
Encephalocele
Occipital Lobe
Neural Tube Defects
Prenatal Diagnosis
2 Citations (Scopus)

Prenatal evaluation with magnetic resonance imaging of a giant blind ectopic ureter associated with a duplex kidney

Chen, C. P., Liu, Y. P., Huang, J. P., Chang, T. Y., Tsai, F-J., Tsai, J. D., Sheu, J. C. & Wang, W., Mar 1 2008, In : Ultrasound in Obstetrics and Gynecology. 31, 3, p. 360-362 3 p.

Research output: Contribution to journalLetter

Ureter
Prenatal Diagnosis
Magnetic Resonance Imaging
Newborn Infant
Kidney

Reply to Zayats et al

Tsai, Y. Y., Chiang, C. C., Wan, L. & Tsai, F-J., Jan 1 2008, In : Eye. 22, 4, 1 p.

Research output: Contribution to journalLetter

1 Citation (Scopus)

Transient abnormal myelopoiesis of mosaic trisomy 21 presenting fetoplacental cytogenetic discrepancy, hepatosplenomegaly, oligohydramnios and abnormal hematological findings

Chen, C. P., Lin, S. P., Tsai, F-J., Lin, H. H., Chern, S. R., Chuang, C. K., Lee, C. C. & Wang, W., Jul 16 2008, In : Genetic Counseling. 19, 2, p. 255-258 4 p.

Research output: Contribution to journalLetter

2006
5 Citations (Scopus)

Androgen receptor gene polymorphism and rheumatoid arthritis in Taiwan [1]

Lo, S. F., Huang, C. M., Tsai, C. H., Chen, W. C., Lai, C. C., Tsai, Y. & Tsai, F-J., Mar 1 2006, In : Clinical and Experimental Rheumatology. 24, 2, p. 209-210 2 p.

Research output: Contribution to journalLetter

Trinucleotide Repeats
Androgen Receptors
Genetic Predisposition to Disease
Taiwan
Rheumatoid Arthritis
7 Citations (Scopus)

Correlation of oestrogen receptor gene polymorphism with gouty arthritis [7]

Huang, C. M., Lo, S. F., Lin, H. C., Chen, M. L., Tsai, C. H. & Tsai, F-J., Dec 1 2006, In : Annals of the rheumatic diseases. 65, 12, p. 1673-1674 2 p.

Research output: Contribution to journalLetter

Polymorphism
Estrogen Receptors
Genes
1 Citation (Scopus)

Gene polymorphisms and bronchopulmonary dysplasia

Lin, H. C., Yeh, T. F. & Tsai, F-J., Oct 1 2006, In : Journal of Pediatrics. 149, 4, 1 p.

Research output: Contribution to journalLetter

Bronchopulmonary Dysplasia
Newborn Infant
Genes
1 Citation (Scopus)

Interleukin-2 receptor gene polymorphism in Chinese patients with systemic lupus erythematosus [1]

Tsai, C. H., Huang, C. M., Lo, S. F., Wan, L. & Tsai, F-J., Aug 1 2006, In : Rheumatology International. 26, 10, p. 949-950 2 p.

Research output: Contribution to journalLetter

Rheumatoid Factor
Interleukin-2 Receptors
Gene Frequency
Systemic Lupus Erythematosus
Case-Control Studies
2005
1 Citation (Scopus)

Angiotensin I-converting enzyme insertion/insertion genotype as a genetic risk factor for cardiovascular disease [1] (multiple letters)

Ogimoto, A., Hamada, M., Miki, T., Higaki, J., Chou, H. T., Tsai, F-J., Tsai, C. H., Zaman, A. G. & Kearney, M. T., Jul 1 2005, In : American Heart Journal. 150, 1

Research output: Contribution to journalLetter

Mitral Valve Prolapse
Peptidyl-Dipeptidase A
Cardiovascular Diseases
Genotype
1 Citation (Scopus)

Association study of gene polymorphism and bronchopulmonary dysplasia [15]

Lin, H. C., Tsai, C. H. & Tsai, F-J., Jan 1 2005, In : Pediatrics. 115, 1, p. 198-199 2 p.

Research output: Contribution to journalLetter

Severity of Illness Index
Bronchopulmonary Dysplasia
Very Low Birth Weight Infant
Genetic Predisposition to Disease
Interleukin-1
12 Citations (Scopus)

Cytokine polymorphisms and chronic lung disease in small preterm infants [4]

Lin, H. C., Tsai, F-J., Tsai, C. H., Hsieh, Y. Y. & Hsu, C. M., Jan 1 2005, In : Archives of Disease in Childhood: Fetal and Neonatal Edition. 90, 1

Research output: Contribution to journalLetter

Infant, Premature, Diseases
Genetic Predisposition to Disease
Premature Infants
Lung Diseases
Chronic Disease
2004
9 Citations (Scopus)

Detection of a homozygous D645E mutation of the acid alpha-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II.

Chen, C. P., Lin, S. P., Tzen, C. Y., Tsai, F-J., Hwu, W. L. & Wang, W., Jan 1 2004, In : Prenatal diagnosis. 24, 3, p. 231-232 2 p.

Research output: Contribution to journalLetter

Glycogen Storage Disease Type II
alpha-Glucosidases
Homozygote
Second Pregnancy Trimester
Lysosomes

Detection of a homozygous D645E mutation of the acid α-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II [3]

Chen, C. P., Lin, S. P., Tzen, C. Y., Tsai, F-J., Hwu, W. L. & Wang, W., Mar 1 2004, In : Prenatal Diagnosis. 24, 3, p. 230-232 3 p.

Research output: Contribution to journalLetter

Glycogen Storage Disease Type III
Glycogen Storage Disease Type II
alpha-Glucosidases
Second Pregnancy Trimester
Glycogen
10 Citations (Scopus)

Febrile Convulsions and Genetic Susceptibility: Role of the Neuronal Nicotinic Acetylcholine Receptor α4 Subunit [1] (multiple letters)

Mulley, J., Heron, S., Scheffer, I., Berkovic, S., Chou, I. C., Tsai, C. H. & Tsai, F-J., May 1 2004, In : Epilepsia. 45, 5, p. 561-562 2 p.

Research output: Contribution to journalLetter

Febrile Seizures
Linkage Disequilibrium
Nicotinic Receptors
Genetic Predisposition to Disease
Gene Frequency
7 Citations (Scopus)

No association of p53 codon 72 and p21 codon 31 polymorphisms in Taiwan Chinese patient's with pterygium [9]

Tsai, Y. Y., Cheng, Y. W., Lee, H., Tseng, S. H., Tsai, C. H. & Tsai, F-J., Jul 1 2004, In : British Journal of Ophthalmology. 88, 7, p. 975-976 2 p.

Research output: Contribution to journalLetter

Cyclin-Dependent Kinase Inhibitor p21
Pterygium
Cyclins
p53 Genes
Taiwan

Significance of Hardy-Weinberg equilibrium in case control (multiple letters)

Bid, H. K., Mittal, R. D., Chen, W. C. & Tsai, F-J., Aug 4 2004, In : Urologia Internationalis. 73, 1, p. 95-96 2 p.

Research output: Contribution to journalLetter

Urinary Calculi
Cadherins
1 Citation (Scopus)

The relationship between insulin-like growth factor-II gene Apa I polymorphism and rheumatoid arthritis

Huang, C. M., Tsai, C. H., Tsai, J. J. P., Kung, P. T., Chen, C. L. & Tsai, F-J., Apr 16 2004, In : Scandinavian Journal of Rheumatology. 33, 2, p. 126-127 2 p.

Research output: Contribution to journalLetter

Insulin-Like Growth Factor II
Gene Expression Regulation
Taiwan
Genetic Markers
Case-Control Studies
2003
15 Citations (Scopus)

Association between polymorphism of interleukin-1 β-511 promoter and susceptibility to febrile convulsions in Taiwanese children [6]

Chou, I. C., Tsai, C. H., Hsieh, Y. Y., Peng, C. T. & Tsai, F-J., Nov 1 2003, In : Acta Paediatrica, International Journal of Paediatrics. 92, 11, 1 p.

Research output: Contribution to journalLetter

Febrile Seizures
Interleukin-1beta
Taiwan
Interleukin-1
Genetic Promoter Regions

Insulin-like growth factor-II gene ApaI polymorphism was not associated with systemic lupus erythematosus [2]

Huang, C. M., Tsai, J. J. P., Tsai, F-J., Chen, W. C. & Chen, C. L., May 31 2003, In : Lupus. 12, 5, p. 423-424 2 p.

Research output: Contribution to journalLetter

Insulin-Like Growth Factor II
Gene Frequency
Systemic Lupus Erythematosus
China
Polymerase Chain Reaction
2 Citations (Scopus)

Prenatal identification of a G338E mutation in FGFR2 in a fetus without sonographic appearance of craniosynostosis [3]

Chen, C. P., Chern, S. R., Lin, S. P., Wang, W. & Tsai, F-J., Feb 1 2003, In : Prenatal Diagnosis. 23, 2, p. 175-176 2 p.

Research output: Contribution to journalLetter

2002
8 Citations (Scopus)

No association of interleukin-4 gene polymorphisms in Chinese patients with rheumatoid arthritis in Taiwan [2]

Huang, C. M., Wu, M. C., Wu, J. Y. & Tsai, F-J., Dec 2002, In : Clinical and Experimental Rheumatology. 20, 6, p. 871-872 2 p.

Research output: Contribution to journalLetter

Genetic Predisposition to Disease
Taiwan
Interleukin-4
China
Rheumatoid Arthritis