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Paternal mosaic inv(20) resulting in a recombinant chromosome 20 in two siblings

Pediatrics international, 2010-06, Vol.52 (3), p.492-495

2010

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Trisomy 13 mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancy

Prenatal diagnosis, 2004-02, Vol.24 (2), p.137-143

2004

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Microchip, reverse transcription-polymerase chain reaction and culture methods to detect enterovirus infection in pediatric patients

Pediatrics international, 2006-02, Vol.48 (1), p.5-10

2006

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A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: possible correlation with poor response to fetal therapy

Prenatal diagnosis, 2008-11, Vol.28 (11), p.1057-1063

2008

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First prenatal exclusion of cystic fibrosis in East Asia

Pediatrics international, 2007-10, Vol.49 (5), p.686-687

2007

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A novel heterozygous missense mutation 377T > C (V126A) of TGIF gene in a family segregated with holoprosencephaly and moyamoya disease

Prenatal diagnosis, 2006-03, Vol.26 (3), p.226-230

2006

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Cytogenetic Analysis of the Formosan Pangolin, Manis Pentadactyla Pentadactyla (Mammalia: Pholidota)

Zoological Studies, 2007-07, Vol.46 (4), p.389-396

2007

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Two novel null mutations in a Taiwanese cystic fibrosis patient and a survey of East Asian CFTR mutations

American journal of medical genetics, 2003-07, Vol.120A (2), p.296-298

2003

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Trisomy 13 manifested as hypoplastic left heart and other structural abnormalities

Prenatal diagnosis, 2003-12, Vol.23 (13), p.1102-1103

2003

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Interstitial Deletion 13q31 Associated with Normal Phenotype: Cytogenetic Study of a Family with Concomitant Segregation of Reciprocal Translocation and Interstitial Deletion

Journal of the Formosan Medical Association, 2007, Vol.106 (7), p.582-588

2007

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Rapid detection of human HLA transgenes in pigs by fluorescence in situ hybridization (FISH) for adjuvant study of human xenotransplantation

Xenotransplantation (Københaven), 2004-09, Vol.11 (5), p.471-475

2004

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Maternal Uniparental Disomy in a Patient with Prader-Willi Syndrome with an Additional Small Inv Dup(15) Chromosome

Journal of the Formosan Medical Association, 2004-12, Vol.103 (12), p.943-947

2004

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Comparison of Immunohistochemical and Fluorescence In Situ Hybridization Assessment for HER-2/neu Status in Taiwanese Breast Cancer Patients

Taiwanese journal of obstetrics & gynecology, 2007, Vol.46 (2), p.146-151

2007

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Detection of Novel CFTR Mutations in Taiwanese Cystic Fibrosis Patients

Journal of the Formosan Medical Association, 2003-05, Vol.102 (5), p.287-291

2003

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Prenatal identification of small supernumerary marker chromosomes by FISH in an infant born with mild congenital anomalies

Prenatal diagnosis, 2006-04, Vol.26 (4), p.383-387

2006

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Antenatal Treatment of Chylothorax and Cystic Hygroma with OK-432 in Nonimmune Hydrops fetalis

Fetal diagnosis and therapy, 2005-07, Vol.20 (4), p.309-315

2005

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Prenatal diagnosis of Machado-Joseph disease/spinocerebellar ataxia type 3 in Taiwan: Early detection of expanded ataxin-3

Journal of clinical laboratory analysis, 2003, Vol.17 (5), p.195-200

2003

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Persistent Fifth Aortic Arch Associated with 22q11.2 Deletion Syndrome

Journal of the Formosan Medical Association, 2006, Vol.105 (4), p.284-289

2006

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Revisit on a distinctive chromosome 1p36 deletion syndrome: report of one case and review of the English literature

International journal of cardiology, 2004-09, Vol.96 (3), p.477-480

2004

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Maternally inherited unbalanced translocation of chromosome 22 in a 5-day-old neonate with persistent fifth aortic arch and tetralogy of Fallot

International journal of cardiology, 2003-08, Vol.90 (2), p.337-339

2003

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Persistent Fifth Aortic Arch Associated with 22q11.2 Deletion Syndrome

Journal of the Formosan Medical Association, 2006-04, Vol.105 (4), p.284-289

2006

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Prenatal Diagnosis of a Fetus Affected with Down Syndrome and Deletion 1p36 Syndrome by Fluorescence in situ Hybridization and Spectral Karyotyping

Fetal diagnosis and therapy, 2004-07, Vol.19 (4), p.356-360

2004

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Observations on wolbachiae in mosquitoes

Journal of invertebrate pathology, 1980-03, Vol.35 (2), p.200-208

1980

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Patient Report: First prenatal exclusion of cystic fibrosis in East Asia

Pediatrics international, 2007-10, Vol.49 (5), p.686

2007

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Original Article: Microchip, reverse transcription-polymerase chain reaction and culture methods to detect enterovirus infection in pediatric patients

Pediatrics international, 2006-02, Vol.48 (1), p.5

2006

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Paternal mosaic inv(20) resulting in a recombinant chromosome 20 in two siblings

Trisomy 13 mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancy

Microchip, reverse transcription-polymerase chain reaction and culture methods to detect enterovirus infection in pediatric patients

A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: possible correlation with poor response to fetal therapy

First prenatal exclusion of cystic fibrosis in East Asia

A novel heterozygous missense mutation 377T > C (V126A) of TGIF gene in a family segregated with holoprosencephaly and moyamoya disease

Cytogenetic Analysis of the Formosan Pangolin, Manis Pentadactyla Pentadactyla (Mammalia: Pholidota)

Two novel null mutations in a Taiwanese cystic fibrosis patient and a survey of East Asian CFTR mutations

Trisomy 13 manifested as hypoplastic left heart and other structural abnormalities

Interstitial Deletion 13q31 Associated with Normal Phenotype: Cytogenetic Study of a Family with Concomitant Segregation of Reciprocal Translocation and Interstitial Deletion

Rapid detection of human HLA transgenes in pigs by fluorescence in situ hybridization (FISH) for adjuvant study of human xenotransplantation

Maternal Uniparental Disomy in a Patient with Prader-Willi Syndrome with an Additional Small Inv Dup(15) Chromosome

Comparison of Immunohistochemical and Fluorescence In Situ Hybridization Assessment for HER-2/neu Status in Taiwanese Breast Cancer Patients

Detection of Novel CFTR Mutations in Taiwanese Cystic Fibrosis Patients

Prenatal identification of small supernumerary marker chromosomes by FISH in an infant born with mild congenital anomalies

Antenatal Treatment of Chylothorax and Cystic Hygroma with OK-432 in Nonimmune Hydrops fetalis

Prenatal diagnosis of Machado-Joseph disease/spinocerebellar ataxia type 3 in Taiwan: Early detection of expanded ataxin-3

Persistent Fifth Aortic Arch Associated with 22q11.2 Deletion Syndrome

Revisit on a distinctive chromosome 1p36 deletion syndrome: report of one case and review of the English literature

Maternally inherited unbalanced translocation of chromosome 22 in a 5-day-old neonate with persistent fifth aortic arch and tetralogy of Fallot

Persistent Fifth Aortic Arch Associated with 22q11.2 Deletion Syndrome

Prenatal Diagnosis of a Fetus Affected with Down Syndrome and Deletion 1p36 Syndrome by Fluorescence in situ Hybridization and Spectral Karyotyping

Observations on wolbachiae in mosquitoes

Patient Report: First prenatal exclusion of cystic fibrosis in East Asia

Original Article: Microchip, reverse transcription-polymerase chain reaction and culture methods to detect enterovirus infection in pediatric patients

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