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Genes
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July 24, 2019
Venous Thromboembolism in Prader-Willi Syndrome: A Questionnaire Survey
Ann M Manzardo, Janalee Heinemann, Barbara McManus, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
April 19, 2022
Central adrenal insufficiency screening with morning plasma cortisol and ACTH levels in Prader-Willi syndrome
Moris A Angulo, Merlin G Butler, Waheeda A Hossain, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2006
A 9-year-old male with a duplication of chromosome 3p25.3p26.2: clinical report and gene expression analysis
Douglas C Bittel, Nataliya Kibiryeva, Majed Dasouki, et al.
Progress in Pediatric Cardiology
|
May 23, 2017
Gene expression in pediatric heart disease with emphasis on conotruncal defects
Douglas C Bittel, Nataliya Kibiryeva, James E O'Brien, et al.
American Journal of Medical Genetics. Part A
|
November 28, 2017
Rare FMR1 gene mutations causing fragile X syndrome: A review
Adam F Sitzmann, Robert T Hagelstrom, Flora Tassone, et al.
International Journal of Molecular Sciences
|
July 21, 2019
High Functioning Autism with Missense Mutations in Synaptotagmin-Like Protein 4 (SYTL4) and Transmembrane Protein 187 (TMEM187) Genes: SYTL4- Protein Modeling, Protein-Protein Interaction, Expression Profiling and MicroRNA Studies
Syed K Rafi, Alberto Fernández-Jaén, Sara Álvarez, et al.
American Journal of Medical Genetics. Part A
|
May 24, 2016
Higher plasma orexin A levels in children with Prader-Willi syndrome compared with healthy unrelated sibling controls
Ann M Manzardo, Lisa Johnson, Jennifer L Miller, et al.
International Journal of Molecular Sciences
|
February 13, 2025
ZEB2 Gene Pathogenic Variants Across Protein-Coding Regions and Impact on Clinical Manifestations: A Review
Waheeda A Hossain, Caroline St Peter, Scott Lovell, et al.
CNS Neuroscience & Therapeutics
|
June 29, 2018
Tobacco and cannabis use in college students are predicted by sex-dimorphic interactions between MAOA genotype and child abuse
Paula J Fite, Shaquanna Brown, Waheeda Hossain, et al.
American Journal of Medical Genetics. Part A
|
December 1, 2015
Elevated plasma oxytocin levels in children with Prader-Willi syndrome compared with healthy unrelated siblings
Lisa Johnson, Ann M Manzardo, Jennifer L Miller, et al.
Page
of 26
Search research articles
Search
Showing results (151-160 of 257) with videos related to
Sort By:
Page
of 26
Genes
|
July 24, 2019
Venous Thromboembolism in Prader-Willi Syndrome: A Questionnaire Survey
Ann M Manzardo, Janalee Heinemann, Barbara McManus, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
April 19, 2022
Central adrenal insufficiency screening with morning plasma cortisol and ACTH levels in Prader-Willi syndrome
Moris A Angulo, Merlin G Butler, Waheeda A Hossain, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2006
A 9-year-old male with a duplication of chromosome 3p25.3p26.2: clinical report and gene expression analysis
Douglas C Bittel, Nataliya Kibiryeva, Majed Dasouki, et al.
Progress in Pediatric Cardiology
|
May 23, 2017
Gene expression in pediatric heart disease with emphasis on conotruncal defects
Douglas C Bittel, Nataliya Kibiryeva, James E O'Brien, et al.
American Journal of Medical Genetics. Part A
|
November 28, 2017
Rare FMR1 gene mutations causing fragile X syndrome: A review
Adam F Sitzmann, Robert T Hagelstrom, Flora Tassone, et al.
International Journal of Molecular Sciences
|
July 21, 2019
High Functioning Autism with Missense Mutations in Synaptotagmin-Like Protein 4 (SYTL4) and Transmembrane Protein 187 (TMEM187) Genes: SYTL4- Protein Modeling, Protein-Protein Interaction, Expression Profiling and MicroRNA Studies
Syed K Rafi, Alberto Fernández-Jaén, Sara Álvarez, et al.
American Journal of Medical Genetics. Part A
|
May 24, 2016
Higher plasma orexin A levels in children with Prader-Willi syndrome compared with healthy unrelated sibling controls
Ann M Manzardo, Lisa Johnson, Jennifer L Miller, et al.
International Journal of Molecular Sciences
|
February 13, 2025
ZEB2 Gene Pathogenic Variants Across Protein-Coding Regions and Impact on Clinical Manifestations: A Review
Waheeda A Hossain, Caroline St Peter, Scott Lovell, et al.
CNS Neuroscience & Therapeutics
|
June 29, 2018
Tobacco and cannabis use in college students are predicted by sex-dimorphic interactions between MAOA genotype and child abuse
Paula J Fite, Shaquanna Brown, Waheeda Hossain, et al.
American Journal of Medical Genetics. Part A
|
December 1, 2015
Elevated plasma oxytocin levels in children with Prader-Willi syndrome compared with healthy unrelated siblings
Lisa Johnson, Ann M Manzardo, Jennifer L Miller, et al.
Page
of 26