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Andrew Dauber

Showing results (21-30 of 144) with videos related to

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Pediatric Annals|March 31, 2025
Rare Disease Growth Monitoring: Improving Early DiagnosisNatasha Shur, Seth Berger, Andrew Dauber, et al.
The Journal of Clinical Endocrinology and Metabolism|July 9, 2018
Insights and Implications of Genome-Wide Association Studies of HeightMichael H Guo, Joel N Hirschhorn, Andrew Dauber
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 6, 2015
Idiopathic short stature due to novel heterozygous mutation of the aggrecan geneJose Bernardo Quintos, Michael H Guo, Andrew Dauber
The Journal of Clinical Endocrinology and Metabolism|April 10, 2024
A Clinical Trial of High-Dose Growth Hormone in a Patient With a Dominant-Negative Growth Hormone Receptor MutationNadia Merchant, Lisa Houchin, Kimberly Boucher, et al.
Pediatric Annals|September 9, 2025
Incorporating Rare Disease Growth Monitoring Into Routine Practice to Improve Early Recognition and Diagnosis of Genetic ConditionsNatasha Shur, Seth Berger, Andrew Dauber, et al.
Pediatric Endocrinology Reviews : PER|May 17, 2017
IMAGe and Related Undergrowth Syndromes: The Complex Spectrum of Gain-of-Function CDKN1C MutationsCatalina Cabrera-Salcedo, Priya Kumar, Vivian Hwa, et al.
American Journal of Medical Genetics. Part A|March 27, 2014
Skeletal dysplasia, global developmental delay, and multiple congenital anomalies in a 5-year-old boy-report of the second family with B3GAT3 mutation and expansion of the phenotypeJulia E von Oettingen, Wen-Hann Tan, Andrew Dauber
Hormone Research in Paediatrics|March 23, 2018
Adrenal Insufficiency, Sex Reversal, and Angelman Syndrome due to Uniparental Disomy Unmasking a Mutation in CYP11A1Ahlee Kim, Masanobu Fujimoto, Vivian Hwa, et al.
Hormone Research in Paediatrics|April 4, 2023
Weekly Growth Hormone (Lonapegsomatropin) Causes Severe Transient Hyperglycemia in a Child with ObesityEinas H Alkhatib, Andrew Dauber, Doris Elizabeth Estrada, et al.
Hormone Research in Paediatrics|May 9, 2013
Isolated central hypothyroidism in young siblings as a manifestation of PROP1 deficiency: clinical impact of whole exome sequencingAri J Wassner, Laurie E Cohen, Eliana Hechter, et al.
Pageof 15

Showing results (21-30 of 144) with videos related to

Sort By:
Pageof 15
Pediatric Annals|March 31, 2025
Rare Disease Growth Monitoring: Improving Early DiagnosisNatasha Shur, Seth Berger, Andrew Dauber, et al.
The Journal of Clinical Endocrinology and Metabolism|July 9, 2018
Insights and Implications of Genome-Wide Association Studies of HeightMichael H Guo, Joel N Hirschhorn, Andrew Dauber
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 6, 2015
Idiopathic short stature due to novel heterozygous mutation of the aggrecan geneJose Bernardo Quintos, Michael H Guo, Andrew Dauber
The Journal of Clinical Endocrinology and Metabolism|April 10, 2024
A Clinical Trial of High-Dose Growth Hormone in a Patient With a Dominant-Negative Growth Hormone Receptor MutationNadia Merchant, Lisa Houchin, Kimberly Boucher, et al.
Pediatric Annals|September 9, 2025
Incorporating Rare Disease Growth Monitoring Into Routine Practice to Improve Early Recognition and Diagnosis of Genetic ConditionsNatasha Shur, Seth Berger, Andrew Dauber, et al.
Pediatric Endocrinology Reviews : PER|May 17, 2017
IMAGe and Related Undergrowth Syndromes: The Complex Spectrum of Gain-of-Function CDKN1C MutationsCatalina Cabrera-Salcedo, Priya Kumar, Vivian Hwa, et al.
American Journal of Medical Genetics. Part A|March 27, 2014
Skeletal dysplasia, global developmental delay, and multiple congenital anomalies in a 5-year-old boy-report of the second family with B3GAT3 mutation and expansion of the phenotypeJulia E von Oettingen, Wen-Hann Tan, Andrew Dauber
Hormone Research in Paediatrics|March 23, 2018
Adrenal Insufficiency, Sex Reversal, and Angelman Syndrome due to Uniparental Disomy Unmasking a Mutation in CYP11A1Ahlee Kim, Masanobu Fujimoto, Vivian Hwa, et al.
Hormone Research in Paediatrics|April 4, 2023
Weekly Growth Hormone (Lonapegsomatropin) Causes Severe Transient Hyperglycemia in a Child with ObesityEinas H Alkhatib, Andrew Dauber, Doris Elizabeth Estrada, et al.
Hormone Research in Paediatrics|May 9, 2013
Isolated central hypothyroidism in young siblings as a manifestation of PROP1 deficiency: clinical impact of whole exome sequencingAri J Wassner, Laurie E Cohen, Eliana Hechter, et al.
Pageof 15