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Jia-Woei Hou

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Taiwan

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Gene Deletion

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Ming-Horng Tsai; Chao-Ping Yang; Peng-Hong Yang; Ming-Chou Chiang; Shih-Ming Chu; Jia-Woei Hou; Jen-Fu Hsu; Hsuan-Rong Huang
Transient myeloproliferative disorder and GATA1 mutation in neonates with and without Down syndrome.
Chien-Min Chen; Chia-Ling Chen; Jia-Woei Hou; Hung-Chih Hsu; Chia-Ying Chung; Shih-Wei Chou; Chu-Hsu Lin; Kai-Hua Chen
Developmental profiles and mentality in preschool children with Prader-Willi syndrome: a preliminary study.
Jia-Woei Hou
Amelioration of hypophosphatemic rickets and osteoporosis with pamidronate and growth hormone in Lowe syndrome.

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2011: Ming-Horng Tsai; Chao-Ping Yang; Peng-Hong Yang; Ming-Chou Chiang; Shih-Ming Chu; Jia-Woei Hou; Jen-Fu Hsu; Hsuan-Rong Huang
Transient myeloproliferative disorder and GATA1 mutation in neonates with and without Down syndrome.
Indian journal of pediatrics 2011;78(7):826-32.
2010: Chien-Min Chen; Chia-Ling Chen; Jia-Woei Hou; Hung-Chih Hsu; Chia-Ying Chung; Shih-Wei Chou; Chu-Hsu Lin; Kai-Hua Chen
Developmental profiles and mentality in preschool children with Prader-Willi syndrome: a preliminary study.
Chang Gung medical journal 2010;33(4):436-42.
2009: Jia-Woei Hou
Amelioration of hypophosphatemic rickets and osteoporosis with pamidronate and growth hormone in Lowe syndrome.
Journal of the Formosan Medical Association = Taiwan yi zhi 2009;108(9):730-5.
2009: Jia-Woei Hou
Changing demography and variable expressivity in autosomal trisomy syndromes.
Pediatrics and neonatology 2009;50(4):133-4.
2009: Jia-Woei Hou
Natural course of neonatal progeroid syndrome.
Pediatrics and neonatology 2009;50(3):102-9.
2009: Chih-Yeu Fang; Chia-Huei Lee; Chung-Chun Wu; Yu-Ting Chang; Shu-Ling Yu; Sheng-Ping Chou; Ping-Ting Huang; Chi-Long Chen; Jia-Woei Hou; Yao Chang; Ching-Hwa Tsai; Kenzo Takada; Jen-Yang Chen
Recurrent chemical reactivations of EBV promotes genome instability and enhances tumor progression of nasopharyngeal carcinoma cells.
International journal of cancer. Journal international du cancer 2009;124(9):2016-25.
2008: Tang-Her Jaing; Shao-Hsuan Hsia; Cheng-Hsun Chiu; Jia-Woei Hou; Chao-Jan Wang; Robert Chow
Successful unrelated cord blood transplantation in a girl with malignant infantile osteopetrosis.
Chinese medical journal 2008;121(13):1245-6.
2008: Jia-Woei Hou
Rapidly progressive scoliosis after successful treatment for osteopenia in Costello syndrome.
American journal of medical genetics. Part A 2008;146(3):393-6.
2008: Sheng-Wen Shaw; Chih-Ping Chen; Po-Jen Cheng; Tzu-Hao Wang; Jia-Woei Hou; Cheng-Tao Lin; Shuenn-Dhy Chang; Hsiao-Lin Hwa; Ju-Li Lin; An-Shine Chao; Yung-Kuei Soong; Fon-Jou Hsieh
Gene dosage change of TPTE and BAGE2 and breakpoint analysis in Robertsonian Down syndrome.
Journal of human genetics 2008;53(2):136-43.
2007: Jung-Ju Huang; Jia-Woei Hou; Ying-Chien Tan; Kuo-Ting Chen; Lun-Jou Lo; Yu-Ray Chen
Van der Woude syndrome: clinical presentation in 64 patients.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2007;44(6):649-52.
2007: Hui-Fang Hsu; Jia-Woei Hou
Variable expressivity in Patau syndrome is not all related to trisomy 13 mosaicism.
American journal of medical genetics. Part A 2007;143A(15):1739-48.
2007: Daisuke Sato; Osamu Shimokawa; Naoki Harada; Oystein E Olsen; Jia-Woei Hou; Wolfgang Muhlbauer; Ellen Blinkenberg; Nobuhiko Okamoto; Akira Kinoshita; Naomichi Matsumoto; Shinji Kondo; Tatsuya Kishino; Nobutomo Miwa; Tadashi Ariga; Norio Niikawa; Koh-ichiro Yoshiura
Congenital arhinia: molecular-genetic analysis of five patients.
American journal of medical genetics. Part A 2007;143(6):546-52.
2007: Rong-Long Chen; Jia-Woei Hou; Pau-Yuan Chang; Fuu-Jen Tsai; Pen-Jung Wang
Matched unrelated bone marrow transplantation without splenectomy for a child with Gaucher disease caused by homozygosity of the L444P mutation, who also suffered from schizencephaly.
Journal of pediatric hematology/oncology 2007;29(1):57-9.
2006: Jia-Woei Hou
Atlantoaxial subluxation with recurrent consciousness disturbance in a boy with Lesch-Nyhan syndrome.
Acta paediatrica (Oslo, Norway : 1992) 2006;95(11):1500-4.
2006: Jia-Woei Hou
Chromosome 10q24.3-qter deletion associated with left-sided first branchial arch defect, diaphragmatic eventration, and duplicated renal pelvis.
American journal of medical genetics. Part A 2006;140(20):2241-4.
2006: Tang-Her Jaing; Jia-Woei Hou; Shih-Hsiang Chen; I-Anne Huang; Chao-Jan Wang; Wen-I Lee
Successful unrelated mismatched cord blood transplantation in a child with malignant infantile osteopetrosis.
Pediatric transplantation 2006;10(5):629-31.
2006: Jia-Woei Hou
Progressive osseous heteroplasia controlled by intravenous administration of pamidronate.
American journal of medical genetics. Part A 2006;140(8):910-3.
2006: Shu-Mei Wang; Jia-Woei Hou; Ju-Li Lin
A retrospective epidemiological and etiological study of metabolic disorders in children with cardiomyopathies.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2006;47(2):83-7.
2006: Noriko Miyake; Osamu Shimokawa; Naoki Harada; Nadiya Sosonkina; Aiko Okubo; Hiroki Kawara; Nobuhiko Okamoto; Hirofumi Ohashi; Kenji Kurosawa; Kenji Naritomi; Tadashi Kaname; Toshiro Nagai; Vorasuk Shotelersuk; Jia-Woei Hou; Yoshimitsu Fukushima; Tatsuro Kondoh; Tadashi Matsumoto; Toshihiko Shinoki; Mitsuhiro Kato; Hidefumi Tonoki; Masayo Nomura; Koh-ichiro Yoshiura; Tatsuya Kishino; Tohru Ohta; Norio Niikawa; Naomichi Matsumoto
No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patients.
American journal of medical genetics. Part A 2006;140(3):291-3.
2005: Jia-Woei Hou
Trisomy chromosome (22)(q13.1-qter) as a result of paternal inversion (22)(p11q13.1) proved using region-specific FISH probes.
Chang Gung medical journal 2005;28(9):657-61.
2005: Jia-Woei Hou
Detection of gene deletions in children with chondrodysplasia punctata, ichthyosis, Kallmann syndrome, and ocular albinism by FISH studies.
Chang Gung medical journal 2005;28(9):643-50.
2005: Jia-Woei Hou; Shiu-Feng Huang
Recurrent panniculitis associated with generalized lipodystrophy and growth hormone deficiency.
Journal of the Formosan Medical Association = Taiwan yi zhi 2005;104(7):518-21.
2005: Jia-Woei Hou
Rubinstein-Taybi syndrome: clinical and molecular cytogenetic studies.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2005;46(3):143-8.
2005: Jia-Woei Hou
Hyperammonemia in neonates: a transient phenomenon or an early sign of inborn errors of metabolism?
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2005;46(2):59-60.
2005: Pen-Jung Wang; Jia-Woei Hou; Whey-Chen Sue; Wang-Tso Lee
Electroclinical characteristics of seizures-comparing Prader--Willi syndrome with Angelman syndrome.
Brain & development 2005;27(2):101-7.
2004: Jia-Woei Hou
Congenital arhinia with de novo reciprocal translocation, t(3;12)(q13.2;p11.2).
American journal of medical genetics. Part A 2004;130A(2):200-3.
2004: Jia-Woei Hou
Cholelithiasis and pseudocholelithiasis in childhood.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2004;45(5):264.
2004: Jia-Woei Hou
Fetal warfarin syndrome.
Chang Gung medical journal 2004;27(9):691-5.
2004: Jia-Woei Hou
Inherited tandem duplication of the X chromosome: dup(X)(q13.2-q21.2) in a family.
Chang Gung medical journal 2004;27(9):685-90.
2004: Jia-Woei Hou
Bardet-Biedl syndrome initially presenting as McKusick-Kaufman syndrome.
Journal of the Formosan Medical Association = Taiwan yi zhi 2004;103(8):629-32.
2004: Jia-Woei Hou
Long-term follow-up of Marshall-Smith syndrome: report of one case.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2004;45(4):232-5.
2004: Jia-Woei Hou
49, XXXXY syndrome.
Chang Gung medical journal 2004;27(7):551-4.
2004: Jia-Woei Hou
Mosaic ring chromosome 14 and monosomy 14 presenting with growth retardation, epilepsy, and blepharophimosis.
Chang Gung medical journal 2004;27(5):373-8.
2004: Jia-Woei Hou
Variable expressivity in a family with Kabuki make-up (Niikawa-Kuroki) syndrome.
Chang Gung medical journal 2004;27(4):307-11.
2004: Jia-Woei Hou
Partial chromosomal 11q trisomy as an unbalanced result of t(11;13)(q23.1;q34)mat in two sisters.
Journal of the Formosan Medical Association = Taiwan yi zhi 2004;103(3):239-43.
2004: Jia-Woei Hou
Biotin responsive multiple carboxylase deficiency presenting as diabetic ketoacidosis.
Chang Gung medical journal 2004;27(2):129-33.
2004: Jia-Woei Hou
A female infant with hypotonia and cardiomegaly.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2004;45(1):1-3.
2003: Jia-Woei Hou
Chromosomal 10Q26 trisomy resulting from paternal T(9;10)(PTER;Q26.1).
Journal of the Formosan Medical Association = Taiwan yi zhi 2003;102(12):887-92.
2003: Jia-Woei Hou
Your diagnosis. A boy with hepatomegaly, muscle hypertrophy and absence of adipose tissue.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2003;44(4):189-90.
2003: Jia-Woei Hou; Chien-Fang Mai
Restrictive dermopathy in two sisters.
Chang Gung medical journal 2003;26(7):510-4.
2003: Jia-Woei Hou
Smith-Magenis syndrome: report of one case.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2003;44(3):161-4.
2003: Jia-Woei Hou; Tso-Ren Wang
A 20-year follow-up of a male patient with type Ia glycogen storage disease.
Chang Gung medical journal 2003;26(4):283-7.
2003: Chih-Wan Su; Kuang-Lin Lin; Jia-Woei Hou; Shih-Ming Jung; Erh-Chung Zen
Spontaneous recovery from a medulloblastoma by a female with Gorlin-Goltz syndrome.
Pediatric neurology 2003;28(3):231-4.
2003: Jia-Woei Hou
Del (9p) syndrome: report of four cases.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2003;44(1):50-3.
2003: Mei-Ching Yu; Jia-Woei Hou
Pseudohypoaldosteronism presenting as acute gastroenteritis: report of one case.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2003;44(1):44-6.
2003: Jia-Woei Hou
Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation.
Chang Gung medical journal 2003;26(1):48-52.
2002: Jia-Woei Hou
Primary systemic carnitine deficiency presenting as recurrent Reye-like syndrome and dilated cardiomyopathy.
Chang Gung medical journal 2002;25(12):832-7.
2002: Jia-Woei Hou
A boy with long-lasting fever and poor hair growth.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2002;43(4):181-2.
2002: Meng-Hao Chen; Kuo-Su Chen; Jia-Woei Hou; Ching-Chang Lee; Jen-Seng Huang
Coexistence of autosomal dominant polycystic kidney disease and neurofibromatosis: report of a family.
American journal of nephrology 2002;22(4):376-80.
2002: Jia-Woei Hou
Double partial monosomies (10p- and Xp-) in a female baby with choanal atresia.
Chang Gung medical journal 2002;25(4):260-5.
2002: Jia-Woei Hou
Human DNA repair defects: are they predisposing to cancer?
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2002;43(1):4-5.
2002: Jia-Woei Hou
A girl with congenital heart defect, deformed hands and a sacral mass.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2002;43(1):1-3.
2001: Jia-Woei Hou
An infant with multiple joint contractures.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2001;42(2):67-8.
2000: Pin Chang; Wen-Yu Tsai; Jia-Woei Hou; Pei-Hung Hsiao; Jing-Shang Lee
Autoimmune thyroiditis in children with Turner syndrome.
Journal of the Formosan Medical Association = Taiwan yi zhi 2000;99(11):823-6.
2000: Pin Chang; Yong-Kwei Tsau; Wen-Yu Tsai; Wei-Shien Tsai; Jia-Woei Hou; Pei-Hung Hsiao; Jing-Shang Lee
Renal malformations in children with Turner's syndrome.
Journal of the Formosan Medical Association = Taiwan yi zhi 2000;99(10):796-8.
2000: Jia-Woei Hou
A newborn with diffuse skin rashes and an occipital mass.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2000;41(5):237-8.
2000: Jia-Woei Hou; W W Tunnessen
Picture of the month. Costello syndrome.
Archives of pediatrics & adolescent medicine 2000;154(6):631-2.
2000: Pi-Feng Chang; SF Huang; Wuh-Liang Hwu; Jia-Woei Hou; Yen-Hsuan Ni; Mei-Hwei Chang
Metabolic disorders mimicking Reye's syndrome.
Journal of the Formosan Medical Association = Taiwan yi zhi 2000;99(4):295-9.
2000: P H Su; Jia-Woei Hou; Wuh-Liang Hwu; Mei-Hwan Wu; Jou-Kou Wang; Tso-Ren Wang
Congenital contractural arachnodactyly (Beals syndrome).
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2000;41(2):59-62.
1999: Y C Hsieh; Jia-Woei Hou
Oral-facial-digital syndrome with Y-shaped fourth metacarpals and endocardial cushion defect.
American journal of medical genetics 1999;86(3):278-81.
1999: Jia-Woei Hou; Tso-Ren Wang
Study of human Y chromosome polymorphism in Taiwan.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 1999;40(5):302-4.
1999: Jia-Woei Hou; Wen-Yu Tsai; Tso-Ren Wang
Detection of KAL-1 gene deletion with fluorescence in situ hybridization.
Journal of the Formosan Medical Association = Taiwan yi zhi 1999;98(6):448-51.
1999: S C Lin; Fung-Rong Hu; Jia-Woei Hou; Yu-Tung Yao; Tso-Ren Wang; Por-Tying Hung
Corneal opacity and congenital glaucoma associated with massive heparan sulfaturia: report of one case.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 1999;40(1):46-9.
1998: Jia-Woei Hou; Jou-Kou Wang; Tso-Ren Wang
FISH analysis in both classical and atypical cases of Williams-Beuren syndrome.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui 1998;39(6):398-403.
1998: Jia-Woei Hou; Tso-Ren Wang; Sou-Ming Chuang
An epidemiological and aetiological study of children with intellectual disability in Taiwan.
Journal of intellectual disability research : JIDR 1998;42 ( Pt 2)():137-43.
1998: J H Lin; Jia-Woei Hou; R J Teng; H F Tien; K H Lin
Jacobsen distal 11q deletion syndrome with a myelodysplastic change of hemopoietic cells.
American journal of medical genetics 1998;75(4):341-4.
1998: Jia-Woei Hou; Tso-Ren Wang
Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan.
European journal of pediatrics 1998;157(2):122-7.
1997: H L Hsu; Pei-Hung Hsiao; Jia-Woei Hou; Wen-Yu Tsai; Tso-Ren Wang
Partial DiGeorge anomaly associated with 10p deletion.
Journal of the Formosan Medical Association = Taiwan yi zhi 1997;96(12):996-9.
1997: Jia-Woei Hou; Jou-Kou Wang; Wen-Yu Tsai; CC Chou; Tso-Ren Wang
CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects.
Journal of the Formosan Medical Association = Taiwan yi zhi 1997;96(6):419-23.
1997: Jia-Woei Hou; Tso-Ren Wang
Differentiation of Fanconi anemia from aplastic anemia by chromosomal breakage test.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui 1997;38(2):121-6.
1997: Frank Lu; Jia-Woei Hou; Wei-Shien Tsai; Ru-Jeng Teng; Kuo-Inn Tsou Yau; Tso-Ren Wang
Tricho-rhino-phalangeal syndrome type II associated with epiglottic aplasia and congenital nephrotic syndrome.
Journal of the Formosan Medical Association = Taiwan yi zhi 1997;96(3):217-21.
1997: Jia-Woei Hou; Jou-Kou Wang; Tso-Ren Wang
Microdeletion oe chromosomal region 7Q11.23 in Williams syndrome.
Journal of the Formosan Medical Association = Taiwan yi zhi 1997;96(2):137-40.
1997: Jia-Woei Hou; Pen-Jung Wang; Tso-Ren Wang
Angelman syndrome assessed by neurological and molecular cytogenetic investigations.
Pediatric neurology 1997;16(1):17-22.
1997: Jia-Woei Hou; Tso-Ren Wang
Primed in situ (PRINS) labeling for rapid detection of numeric and structural chromosome anomalies.
Journal of the Formosan Medical Association = Taiwan yi zhi 1997;96(1):46-50.
1996: Jia-Woei Hou; Tso-Ren Wang
Amelia, dextrocardia, asplenia, and congenital short bowel in deleted ring chromosome 4.
Journal of medical genetics 1996;33(10):879-81.
1996: S C Chuang; Wuh-Liang Hwu; C C Wu; Jia-Woei Hou; Tso-Ren Wang
Diagnosis of mucopolysaccharidosis type IIIB.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui 1996;37(5):320-3.
1996: Jia-Woei Hou; Tso-Ren Wang
Chromosomal rearrangements detected by FISH and G-banding.
Journal of the Formosan Medical Association = Taiwan yi zhi 1996;95(9):686-91.
1996: Jia-Woei Hou; Shi-Ping Chou; Tso-Ren Wang
Metabolic function and liver histopathology in Reye-like illnesses.
Acta paediatrica (Oslo, Norway : 1992) 1996;85(9):1053-7.
1996: Chun-Yi Lu; Jia-Woei Hou; Pen-Jung Wang; Hsiu-Hui Chiu; Tso-Ren Wang
Homocystinuria presenting as fatal common carotid artery occlusion.
Pediatric neurology 1996;15(2):159-62.
1996: Jia-Woei Hou; Tso-Ren Wang
Prader-Willi syndrome: clinical and molecular cytogenetic investigations.
Journal of the Formosan Medical Association = Taiwan yi zhi 1996;95(6):474-9.
1996: Jia-Woei Hou; Tso-Ren Wang
Double aneuploidy with Down's-Klinefelter's syndrome.
Journal of the Formosan Medical Association = Taiwan yi zhi 1996;95(4):350-2.
1996: Jia-Woei Hou; Tso-Ren Wang
Amino acid and DNA analyses in a family with ornithine transcarbamylase deficiency.
Journal of the Formosan Medical Association = Taiwan yi zhi 1996;95(2):144-7.
1996: S F Gau; Wei-Tsuen Soong; H M Liu; Jia-Woei Hou; Wen-Yu Tsai; Yen-Nan Chiu; Y C Yeh; Pen-Jung Wang; Tso-Ren Wang
Kleine-Levin syndrome in a boy with Prader-Willi syndrome.
Sleep 1996;19(1):13-7.
1995: Jia-Woei Hou; Tso-Ren Wang
Galloway-Mowat syndrome in Taiwan.
American journal of medical genetics 1995;58(3):245-8.
1995: Jia-Woei Hou; Tso-Ren Wang
Molecular cytogenetic studies of duplication 9q32-->q34.3 inserted into 9q13.
Clinical genetics 1995;48(3):148-50.
1995: Jia-Woei Hou; Tso-Ren Wang
Transient tyrosinemia presenting as lactic acidosis in a term baby: report of one case.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui 1995;36(3):217-20.
1995: Jia-Woei Hou; Tso-Ren Wang
Idiopathic juvenile osteoporosis: five-year case follow-up.
Journal of the Formosan Medical Association = Taiwan yi zhi 1995;94(5):277-80.
1995: Jia-Woei Hou; Jou-Kou Wang; C C Chou; Tso-Ren Wang
Microdeletion of chromosomal region 22q11 in DiGeorge syndrome: report of a case.
Journal of the Formosan Medical Association = Taiwan yi zhi 1995;94(4):200-2.
1995: Jia-Woei Hou; Tso-Ren Wang
3-Methylglutaconic aciduria presenting as Reye syndrome in a Chinese boy.
Journal of inherited metabolic disease 1995;18(5):645-6.
1995: Jia-Woei Hou; Tso-Ren Wang
Methylmalonic aciduria and urolithiasis in a Chinese boy with untreated phenylketonuria.
Journal of inherited metabolic disease 1995;18(1):79-80.
1995: Wang-Tso Lee; Jia-Woei Hou; Kuo-Inn Tsou Yau; Tso-Ren Wang
Trisomy 18 in a patient with CHARGE association.
Journal of the Formosan Medical Association = Taiwan yi zhi 1995;94(1-2):60-2.
1994: Jia-Woei Hou; Tso-Ren Wang
Cytogenetic investigations in trisomy 21 with reciprocal 4/9 translocation: report of a case.
Journal of the Formosan Medical Association = Taiwan yi zhi 1994;93(11-12):958-60.
1994: Jia-Woei Hou; Pen-Jung Wang; Tso-Ren Wang
Tuberous sclerosis in children.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui 1994;35(2):102-7.
1994: Jia-Woei Hou; C H Liu; Tso-Ren Wang
Molecular cytogenetic studies of children with marker chromosomes.
Journal of the Formosan Medical Association = Taiwan yi zhi 1994;93(3):205-9.
1994: Jia-Woei Hou; Tso-Ren Wang
Pyridoxine-responsive homocystinuria with ruptured sinus of Valsalva in a Chinese boy.
Journal of inherited metabolic disease 1994;17(6):759.
1993: Tso-Ren Wang; Wuh-Liang Hwu; Jia-Woei Hou; H M Tsai; C H Liu
Y-specific polymerase chain reaction for the interpretation of a chromosome marker.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui 1993;34(2):113-7.
1993: Tso-Ren Wang; Wuh-Liang Hwu; Jia-Woei Hou; Shi-Ping Chou; C H Liu
Fragile-X mental retardation--a combination of cytogenetic and molecular approaches, with greater emphasis on DNA analysis.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui 1993;34(2):105-12.
1993: Jia-Woei Hou; Wuh-Liang Hwu; Wen-Yu Tsai; Jing-Shang Lee; Tso-Ren Wang; Hung-Chi Lue
Cardiovascular disorders in Turner's syndrome and its correlation to karyotype.
Journal of the Formosan Medical Association = Taiwan yi zhi 1993;92(2):188-9.
1992: Jia-Woei Hou; C H Liu; Tso-Ren Wang; H M Zhu; S Jiang; L J Sciorra; M L Lee
Mosaic ring chromosome 13 analyzed by fluorescence in situ hybridization: report of a case.
Journal of the Formosan Medical Association = Taiwan yi zhi 1992;91(11):1108-11.
1992: Jia-Woei Hou; Y J Lin; Pen-Jung Wang; Tso-Ren Wang
Atlantoaxial subluxation and syringomyelia in Down syndrome: report of one case.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui 1992;33(6):423-7.
1992: Jia-Woei Hou; M L Lee; Tso-Ren Wang
Identification of sex chromosomal abnormalities by fluorescence in situ hybridization.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui 1992;33(5):332-40.
1990: Dong-Tsamn Lin; Jia-Woei Hou; K H Lin; W M Chuu; Kuo-Sin Lin
Clinical observation of Wilms' tumor.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui 1990;31(5):299-306.
1990: Tso-Ren Wang; Jia-Woei Hou; H M Tsai
Restriction fragment length polymorphisms at the methylmalonyl CoA mutase locus in normal Chinese.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui 1990;31(5):275-9.
1990: Jia-Woei Hou; Tso-Ren Wang
Isovaleric acidemia: report of one case.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui 1990;31(4):262-5.
1990: Tso-Ren Wang; Jia-Woei Hou; H M Tsai
Restriction fragment length polymorphisms at the ornithine transcarbamylase locus in normal Chinese.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui 1990;31(4):221-5.