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Julian C Lui

Showing results (41-50 of 51) with videos related to

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Frontiers in Endocrinology|July 1, 2021
Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary GenesBirgit Weiss, Birgit Eberle, Ralph Roeth, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 25, 2026
A cartilage-targeted IGF-1-antibody fusion protein as a new therapeutic approach for IGF-1 deficiencyKrishma Tailor, Timothy Stowe, Kirtal Hansdah, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 21, 2015
Mice Deficient in AKAP13 (BRX) Are Osteoporotic and Have Impaired OsteogenesisHisashi Koide, Kenn Holmbeck, Julian C Lui, et al.
Frontiers in Immunology|April 8, 2017
Unexpected Cartilage Phenotype in CD4-Cre-Conditional SOS-Deficient MiceGeoffrey Guittard, Devorah L Gallardo, Wenmei Li, et al.
The Journal of Clinical Endocrinology and Metabolism|August 31, 2012
Novel microcephalic primordial dwarfism disorder associated with variants in the centrosomal protein nineinAndrew Dauber, Stephen H Lafranchi, Zoltan Maliga, et al.
Nature Communications|January 20, 2015
Biological interpretation of genome-wide association studies using predicted gene functionsTune H Pers, Juha M Karjalainen, Yingleong Chan, et al.
Hormone Research in Paediatrics|October 11, 2014
Copy number variants in short children born small for gestational ageJan M Wit, Hermine A van Duyvenvoorde, Jan B van Klinken, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2020
DLG2 variants in patients with pubertal disordersYoun Hee Jee, Sehoon Won, Julian C Lui, et al.
European Journal of Human Genetics : EJHG|September 26, 2013
Copy number variants in patients with short statureHermine A van Duyvenvoorde, Julian C Lui, Sarina G Kant, et al.
Genetics in Medicine Open|March 25, 2025
Variants in <i>WASHC3</i>, a component of the WASH complex, cause short stature, variable neurodevelopmental abnormalities, and distinctive facial dysmorphismYoun Hee Jee, Julian C Lui, Dana Marafi, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Frontiers in Endocrinology|July 1, 2021
Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary GenesBirgit Weiss, Birgit Eberle, Ralph Roeth, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 25, 2026
A cartilage-targeted IGF-1-antibody fusion protein as a new therapeutic approach for IGF-1 deficiencyKrishma Tailor, Timothy Stowe, Kirtal Hansdah, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 21, 2015
Mice Deficient in AKAP13 (BRX) Are Osteoporotic and Have Impaired OsteogenesisHisashi Koide, Kenn Holmbeck, Julian C Lui, et al.
Frontiers in Immunology|April 8, 2017
Unexpected Cartilage Phenotype in CD4-Cre-Conditional SOS-Deficient MiceGeoffrey Guittard, Devorah L Gallardo, Wenmei Li, et al.
The Journal of Clinical Endocrinology and Metabolism|August 31, 2012
Novel microcephalic primordial dwarfism disorder associated with variants in the centrosomal protein nineinAndrew Dauber, Stephen H Lafranchi, Zoltan Maliga, et al.
Nature Communications|January 20, 2015
Biological interpretation of genome-wide association studies using predicted gene functionsTune H Pers, Juha M Karjalainen, Yingleong Chan, et al.
Hormone Research in Paediatrics|October 11, 2014
Copy number variants in short children born small for gestational ageJan M Wit, Hermine A van Duyvenvoorde, Jan B van Klinken, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2020
DLG2 variants in patients with pubertal disordersYoun Hee Jee, Sehoon Won, Julian C Lui, et al.
European Journal of Human Genetics : EJHG|September 26, 2013
Copy number variants in patients with short statureHermine A van Duyvenvoorde, Julian C Lui, Sarina G Kant, et al.
Genetics in Medicine Open|March 25, 2025
Variants in <i>WASHC3</i>, a component of the WASH complex, cause short stature, variable neurodevelopmental abnormalities, and distinctive facial dysmorphismYoun Hee Jee, Julian C Lui, Dana Marafi, et al.
Pageof 6