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Taiwanese Journal of Obstetrics & Gynecology
|
August 17, 2010
Apert syndrome associated with upper airway obstruction and gastroesophageal reflux inducing polyhydramnios in the third trimester
Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, et al.
Orphanet Journal of Rare Diseases
|
February 12, 2014
Natural history and clinical assessment of Taiwanese patients with mucopolysaccharidosis IVA
Hsiang-Yu Lin, Chih-Kuang Chuang, Ming-Ren Chen, et al.
International Journal of Medical Sciences
|
October 4, 2023
22q11.2 Deletion Syndrome in Taiwan: Clinical Presentation and Immune System Status of Patients
Chung-Lin Lee, Shan-Miao Lin, Ming-Ren Chen, et al.
Annals of Human Genetics
|
January 5, 2011
Genetic studies of Prader-Willi patients provide evidence for conservation of genomic architecture in proximal chromosome 15q
Aihua Hou, Shuan-Pei Lin, Shi Yun Ho, et al.
Pediatric Pulmonology
|
August 19, 2010
Polysomnographic characteristics in patients with mucopolysaccharidoses
Hsiang-Yu Lin, Ming-Ren Chen, Ching-Chi Lin, et al.
International Journal of Medical Sciences
|
September 15, 2021
Otorhinolaryngological Management in Taiwanese Patients with Mucopolysaccharidoses
Chung-Lin Lee, Kuo-Sheng Lee, Chih-Kuang Chuang, et al.
Diagnostics (Basel, Switzerland)
|
August 29, 2024
Genetic and Phenotypic Spectrum of <i>KMT2D</i> Variants in Taiwanese Case Series of Kabuki Syndrome
Chung-Lin Lee, Chih-Kuang Chuang, Ming-Ren Chen, et al.
Clinical Chemistry
|
October 17, 2006
Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: Application in Prader-Willi syndrome and Duchenne muscular dystrophy
Chia-Cheng Hung, Chih-Ping Chen, Shuan-Pei Lin, et al.
Pediatrics and Neonatology
|
December 25, 2018
Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in Taiwan
Chung-Lin Lee, Chen-Hao Lee, Chih-Kuang Chuang, et al.
Diagnostics (Basel, Switzerland)
|
April 26, 2024
Illuminating the Genetic Basis of Congenital Heart Disease in Patients with Kabuki Syndrome
Chung-Lin Lee, Chih-Kuang Chuang, Ming-Ren Chen, et al.
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of 29
Search research articles
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Showing results (181-190 of 281) with videos related to
Sort By:
Page
of 29
Taiwanese Journal of Obstetrics & Gynecology
|
August 17, 2010
Apert syndrome associated with upper airway obstruction and gastroesophageal reflux inducing polyhydramnios in the third trimester
Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, et al.
Orphanet Journal of Rare Diseases
|
February 12, 2014
Natural history and clinical assessment of Taiwanese patients with mucopolysaccharidosis IVA
Hsiang-Yu Lin, Chih-Kuang Chuang, Ming-Ren Chen, et al.
International Journal of Medical Sciences
|
October 4, 2023
22q11.2 Deletion Syndrome in Taiwan: Clinical Presentation and Immune System Status of Patients
Chung-Lin Lee, Shan-Miao Lin, Ming-Ren Chen, et al.
Annals of Human Genetics
|
January 5, 2011
Genetic studies of Prader-Willi patients provide evidence for conservation of genomic architecture in proximal chromosome 15q
Aihua Hou, Shuan-Pei Lin, Shi Yun Ho, et al.
Pediatric Pulmonology
|
August 19, 2010
Polysomnographic characteristics in patients with mucopolysaccharidoses
Hsiang-Yu Lin, Ming-Ren Chen, Ching-Chi Lin, et al.
International Journal of Medical Sciences
|
September 15, 2021
Otorhinolaryngological Management in Taiwanese Patients with Mucopolysaccharidoses
Chung-Lin Lee, Kuo-Sheng Lee, Chih-Kuang Chuang, et al.
Diagnostics (Basel, Switzerland)
|
August 29, 2024
Genetic and Phenotypic Spectrum of <i>KMT2D</i> Variants in Taiwanese Case Series of Kabuki Syndrome
Chung-Lin Lee, Chih-Kuang Chuang, Ming-Ren Chen, et al.
Clinical Chemistry
|
October 17, 2006
Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: Application in Prader-Willi syndrome and Duchenne muscular dystrophy
Chia-Cheng Hung, Chih-Ping Chen, Shuan-Pei Lin, et al.
Pediatrics and Neonatology
|
December 25, 2018
Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in Taiwan
Chung-Lin Lee, Chen-Hao Lee, Chih-Kuang Chuang, et al.
Diagnostics (Basel, Switzerland)
|
April 26, 2024
Illuminating the Genetic Basis of Congenital Heart Disease in Patients with Kabuki Syndrome
Chung-Lin Lee, Chih-Kuang Chuang, Ming-Ren Chen, et al.
Page
of 29