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Prenatal exposure to phthalate esters and behavioral syndromes in children at 8 years of age: Taiwan Maternal and Infant Cohort Study

Environmental health perspectives, 2015-01, Vol.123 (1), p.95-100

2015

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Thyroid and growth hormone concentrations in 8-year-old children exposed in utero to dioxins and polychlorinated biphenyls

The Journal of Toxicological Sciences, 2015/06/01, Vol.40(3), pp.309-319

2015

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Development of Genetic Counseling Services in Taiwan

Journal of genetic counseling, 2013-12, Vol.22 (6), p.839-843

2013

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Herlyn-Werner-Wunderlich Syndrome Consisting of Uterine Didelphys, Obstructed Hemivagina and Ipsilateral Renal Agenesis in a Newborn

Pediatrics and neonatology, 2012-02, Vol.53 (1), p.68-71

2012

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A MID1 gene mutation in a patient with Opitz G/BBB syndrome that altered the 3D structure of SPRY domain

American journal of medical genetics. Part A, 2012-04, Vol.158A (4), p.726-731

2012

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Taiwanese Nursing Students' Perceived Knowledge and Clinical Comfort With Genetics

Journal of nursing scholarship, 2011-06, Vol.43 (2), p.125-132

2011

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Leptin expression and leptin receptor gene polymorphisms in growth hormone deficiency patients

Human genetics, 2011-04, Vol.129 (4), p.455-462

2011

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Siblings With Deletion 22q13.3 and Trisomy 15q26 Inherited From a Maternally Balanced Translocation

Pediatrics and neonatology, 2011-10, Vol.52 (5), p.287-289

2011

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De Novo Interstitial Deletion of Chromosome 2 (p23p24)

Pediatrics and neonatology, 2011-02, Vol.52 (1), p.46-50

2011

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Hydranencephaly Associated with Interruption of Bilateral Internal Carotid Arteries

Pediatrics and neonatology, 2008-04, Vol.49 (2), p.43-47

2008

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Ocular Findings in a Case of Trisomy 18 With Variant of Dandy-Walker Syndrome

Pediatrics and neonatology, 2010-10, Vol.51 (5), p.292-295

2010

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Interstitial Deletions of the Short Arm of Chromosome 4 in a Patient With Mental Retardation and Focal Seizure

Pediatrics and neonatology, 2011-06, Vol.52 (3), p.165-168

2011

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Trisomy 18 Syndrome with Incomplete Cantrell Syndrome

Pediatrics and neonatology, 2008-06, Vol.49 (3), p.84-87

2008

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Sacral Dysgenesis Associated with Terminal Deletion of Chromosome 7 (q36-qter)

Pediatrics and neonatology, 2008-10, Vol.49 (5), p.189-192

2008

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Successful Weaning of a Laryngeal Mask Airway After a Tongue-lip Adhesion Operation in a Case With Cerebro-costo-mandibular Syndrome

Pediatrics and neonatology, 2010-02, Vol.51 (1), p.57-60

2010

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Study of leptin levels and gene polymorphisms in patients with central precocious puberty

Pediatric research, 2012-04, Vol.71 (1-4), p.361-367

2012

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Treacher Collins Syndrome with a de Novo 5-bp Deletion in the TCOF1 Gene

Journal of the Formosan Medical Association, 2006, Vol.105 (6), p.518-521

2006

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Pfeiffer-like Syndrome With Holoprosencephaly: A Newborn With Maternal Smoking and Alcohol Exposure

Pediatrics and neonatology, 2009-10, Vol.50 (5), p.234-238

2009

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Terminal Deletion of Chromosome 6q

Pediatrics and neonatology, 2008-06, Vol.49 (3), p.88-93

2008

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Perceived knowledge and clinical comfort with genetics among Taiwanese nurses enrolled in a RN-to-BSN program

Nurse education today, 2013-08, Vol.33 (8), p.802-807

2013

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Identification of a novel mutation and polymorphic change in the NIPBL gene of subjects with Cornelia de Lange syndrome

Genes & Genomics, 2008, 30(3), , pp.253-260

2008

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A polymorphism in the leptin receptor gene at position 223 is associated with growth hormone replacement therapy responsiveness in idiopathic short stature and growth hormone deficiency patients

European journal of medical genetics, 2012-12, Vol.55 (12), p.682-687

2012

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Study of the leptin levels and its gene polymorphisms in patients with idiopathic short stature and growth hormone deficiency

Endocrine, 2012-08, Vol.42 (1), p.196-204

2012

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A case of a Taiwanese patient with cleidocranial dysplasia possessing a de novo mutation of RUNX2 gene

Genes & Genomics, 2008, 30(4), , pp.383-388

2008

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Six Cases of Deletion 9p24 and Trisomy 19q13.4 Inherited from a Familial Balanced Translocation

Journal of the Formosan Medical Association, 2005-07, Vol.104 (7), p.525-530

2005

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Prenatal exposure to phthalate esters and behavioral syndromes in children at 8 years of age: Taiwan Maternal and Infant Cohort Study

Thyroid and growth hormone concentrations in 8-year-old children exposed in utero to dioxins and polychlorinated biphenyls

Development of Genetic Counseling Services in Taiwan

Herlyn-Werner-Wunderlich Syndrome Consisting of Uterine Didelphys, Obstructed Hemivagina and Ipsilateral Renal Agenesis in a Newborn

A MID1 gene mutation in a patient with Opitz G/BBB syndrome that altered the 3D structure of SPRY domain

Taiwanese Nursing Students' Perceived Knowledge and Clinical Comfort With Genetics

Leptin expression and leptin receptor gene polymorphisms in growth hormone deficiency patients

Siblings With Deletion 22q13.3 and Trisomy 15q26 Inherited From a Maternally Balanced Translocation

De Novo Interstitial Deletion of Chromosome 2 (p23p24)

Hydranencephaly Associated with Interruption of Bilateral Internal Carotid Arteries

Ocular Findings in a Case of Trisomy 18 With Variant of Dandy-Walker Syndrome

Interstitial Deletions of the Short Arm of Chromosome 4 in a Patient With Mental Retardation and Focal Seizure

Trisomy 18 Syndrome with Incomplete Cantrell Syndrome

Sacral Dysgenesis Associated with Terminal Deletion of Chromosome 7 (q36-qter)

Successful Weaning of a Laryngeal Mask Airway After a Tongue-lip Adhesion Operation in a Case With Cerebro-costo-mandibular Syndrome

Study of leptin levels and gene polymorphisms in patients with central precocious puberty

Treacher Collins Syndrome with a de Novo 5-bp Deletion in the TCOF1 Gene

Pfeiffer-like Syndrome With Holoprosencephaly: A Newborn With Maternal Smoking and Alcohol Exposure

Terminal Deletion of Chromosome 6q

Perceived knowledge and clinical comfort with genetics among Taiwanese nurses enrolled in a RN-to-BSN program

Identification of a novel mutation and polymorphic change in the NIPBL gene of subjects with Cornelia de Lange syndrome

A polymorphism in the leptin receptor gene at position 223 is associated with growth hormone replacement therapy responsiveness in idiopathic short stature and growth hormone deficiency patients

Study of the leptin levels and its gene polymorphisms in patients with idiopathic short stature and growth hormone deficiency

A case of a Taiwanese patient with cleidocranial dysplasia possessing a de novo mutation of RUNX2 gene

Six Cases of Deletion 9p24 and Trisomy 19q13.4 Inherited from a Familial Balanced Translocation

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