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Journal of Movement Disorders
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March 19, 2020
Dopa-Responsive Dystonia: A Male Patient Inherited a Novel GCH1 Deletion from an Asymptomatic Mother
Wendi Wang, Baozhong Xin, Heng Wang
Frontiers in Genetics
|
June 7, 2021
From Disease Description and Gene Discovery to Functional Cell Pathway: A Decade-Long Journey for TMCO1
Helen Batchelor-Regan, Baozhong Xin, Aimin Zhou, et al.
Journal of Pediatric Health Care : Official Publication of National Association of Pediatric Nurse Associates & Practitioners
|
March 12, 2017
Congenital Glucose-Galactose Malabsorption: A Case Report
Sharon Anderson, Soula Koniaris, Baozhong Xin, et al.
Journal of Medicinal Food
|
July 27, 2007
Trophic effect of bee pollen on small intestine in broiler chickens
Jue Wang, Shenghe Li, Qifa Wang, et al.
American Journal of Medical Genetics. Part A
|
October 17, 2007
Homozygosity for a novel splice site mutation in the cardiac myosin-binding protein C gene causes severe neonatal hypertrophic cardiomyopathy
Baozhong Xin, Erik Puffenberger, John Tumbush, et al.
American Journal of Medical Genetics. Part A
|
February 26, 2013
Cutaneous dyspigmentation in patients with ganglioside GM3 synthase deficiency
Heng Wang, Alicia Bright, Baozhong Xin, et al.
Archives of Neurology
|
April 17, 2008
Lack of spartin protein in Troyer syndrome: a loss-of-function disease mechanism?
Joanna C Bakowska, Heng Wang, Baozhong Xin, et al.
Ophthalmic Genetics
|
October 3, 2024
Ectopia lentis associated with a 20-base deletion in the <i>ADAMTSL4</i> gene in the Old Order Amish population
Grace Kuang, Baozhong Xin, Valerie Sency, et al.
The Journal of Allergy and Clinical Immunology
|
November 9, 2025
Utilization of the All of Us Research Program in a study of genetics in Yao syndrome
Song Wu, Zuoming Deng, Asif Uddin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 19, 2009
Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation
Baozhong Xin, Erik G Puffenberger, Susan Turben, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 28) with videos related to
Sort By:
Page
of 3
Journal of Movement Disorders
|
March 19, 2020
Dopa-Responsive Dystonia: A Male Patient Inherited a Novel GCH1 Deletion from an Asymptomatic Mother
Wendi Wang, Baozhong Xin, Heng Wang
Frontiers in Genetics
|
June 7, 2021
From Disease Description and Gene Discovery to Functional Cell Pathway: A Decade-Long Journey for TMCO1
Helen Batchelor-Regan, Baozhong Xin, Aimin Zhou, et al.
Journal of Pediatric Health Care : Official Publication of National Association of Pediatric Nurse Associates & Practitioners
|
March 12, 2017
Congenital Glucose-Galactose Malabsorption: A Case Report
Sharon Anderson, Soula Koniaris, Baozhong Xin, et al.
Journal of Medicinal Food
|
July 27, 2007
Trophic effect of bee pollen on small intestine in broiler chickens
Jue Wang, Shenghe Li, Qifa Wang, et al.
American Journal of Medical Genetics. Part A
|
October 17, 2007
Homozygosity for a novel splice site mutation in the cardiac myosin-binding protein C gene causes severe neonatal hypertrophic cardiomyopathy
Baozhong Xin, Erik Puffenberger, John Tumbush, et al.
American Journal of Medical Genetics. Part A
|
February 26, 2013
Cutaneous dyspigmentation in patients with ganglioside GM3 synthase deficiency
Heng Wang, Alicia Bright, Baozhong Xin, et al.
Archives of Neurology
|
April 17, 2008
Lack of spartin protein in Troyer syndrome: a loss-of-function disease mechanism?
Joanna C Bakowska, Heng Wang, Baozhong Xin, et al.
Ophthalmic Genetics
|
October 3, 2024
Ectopia lentis associated with a 20-base deletion in the <i>ADAMTSL4</i> gene in the Old Order Amish population
Grace Kuang, Baozhong Xin, Valerie Sency, et al.
The Journal of Allergy and Clinical Immunology
|
November 9, 2025
Utilization of the All of Us Research Program in a study of genetics in Yao syndrome
Song Wu, Zuoming Deng, Asif Uddin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 19, 2009
Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation
Baozhong Xin, Erik G Puffenberger, Susan Turben, et al.
Page
of 3