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Gary Bellus

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American Journal of Medical Genetics. Part A|September 21, 2011
Identical twin sisters with Rubinstein-Taybi syndrome associated with Chiari malformations and syrinxLea Parsley, Gary Bellus, Michael Handler, et al.
Pediatric Dermatology|February 29, 2020
Diagnosis of pili trianguli et canaliculi by frozen section: A rapid and inexpensive method of diagnosisAmanda Krenitsky, Audrey Dean, Christina DiCarlo, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
Mesomelic and rhizomelic short stature: The phenotype of combined Leri-Weill dyschondrosteosis and achondroplasia or hypochondroplasiaJudith L Ross, Gary Bellus, Charles I Scott, et al.
The Journal of Craniofacial Surgery|September 22, 2010
Male with mosaicism for supernumerary ring X chromosome: analysis of phenotype and characterization of genotype using array comparative genome hybridizationPeter R Baker, Anne Chun-Hui Tsai, Michelle Springer, et al.
Cold Spring Harbor Molecular Case Studies|May 22, 2021
Neurodevelopmental phenotypes in individuals with pathogenic variants in <i>CHAMP1</i>Madison Garrity, Haluk Kavus, Marta Rojas-Vasquez, et al.
Medrxiv : the Preprint Server for Health Sciences|September 24, 2024
Phenotypic Findings Associated with Variation in ElastinAnne Justice, Melissa A Kelly, Gary Bellus, et al.
HGG Advances|November 28, 2024
Phenotypic findings associated with variation in elastinAnne Justice, Melissa A Kelly, Gary Bellus, et al.
American Journal of Medical Genetics. Part A|May 7, 2011
Identification of SPRED1 deletions using RT-PCR, multiplex ligation-dependent probe amplification and quantitative PCREmily Spencer, Julia Davis, Fady Mikhail, et al.
American Journal of Human Genetics|February 22, 2024
De novo variants in DENND5B cause a neurodevelopmental disorderMarcello Scala, Valeria Tomati, Matteo Ferla, et al.
Frontiers in Cell and Developmental Biology|December 26, 2022
The different clinical facets of <i>SYN1</i>-related neurodevelopmental disordersIlaria Parenti, Elsa Leitão, Alma Kuechler, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics. Part A|September 21, 2011
Identical twin sisters with Rubinstein-Taybi syndrome associated with Chiari malformations and syrinxLea Parsley, Gary Bellus, Michael Handler, et al.
Pediatric Dermatology|February 29, 2020
Diagnosis of pili trianguli et canaliculi by frozen section: A rapid and inexpensive method of diagnosisAmanda Krenitsky, Audrey Dean, Christina DiCarlo, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
Mesomelic and rhizomelic short stature: The phenotype of combined Leri-Weill dyschondrosteosis and achondroplasia or hypochondroplasiaJudith L Ross, Gary Bellus, Charles I Scott, et al.
The Journal of Craniofacial Surgery|September 22, 2010
Male with mosaicism for supernumerary ring X chromosome: analysis of phenotype and characterization of genotype using array comparative genome hybridizationPeter R Baker, Anne Chun-Hui Tsai, Michelle Springer, et al.
Cold Spring Harbor Molecular Case Studies|May 22, 2021
Neurodevelopmental phenotypes in individuals with pathogenic variants in <i>CHAMP1</i>Madison Garrity, Haluk Kavus, Marta Rojas-Vasquez, et al.
Medrxiv : the Preprint Server for Health Sciences|September 24, 2024
Phenotypic Findings Associated with Variation in ElastinAnne Justice, Melissa A Kelly, Gary Bellus, et al.
HGG Advances|November 28, 2024
Phenotypic findings associated with variation in elastinAnne Justice, Melissa A Kelly, Gary Bellus, et al.
American Journal of Medical Genetics. Part A|May 7, 2011
Identification of SPRED1 deletions using RT-PCR, multiplex ligation-dependent probe amplification and quantitative PCREmily Spencer, Julia Davis, Fady Mikhail, et al.
American Journal of Human Genetics|February 22, 2024
De novo variants in DENND5B cause a neurodevelopmental disorderMarcello Scala, Valeria Tomati, Matteo Ferla, et al.
Frontiers in Cell and Developmental Biology|December 26, 2022
The different clinical facets of <i>SYN1</i>-related neurodevelopmental disordersIlaria Parenti, Elsa Leitão, Alma Kuechler, et al.
Pageof 2