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Erwin Brosens

Showing results (51-60 of 72) with videos related to

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International Journal of Molecular Sciences|November 27, 2021
The Somatic Mutation Paradigm in Congenital Malformations: Hirschsprung Disease as a ModelKatherine C MacKenzie, Rhiana Garritsen, Rajendra K Chauhan, et al.
Gastroenterology|March 31, 2018
Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung DiseaseYunia Sribudiani, Rajendra K Chauhan, Maria M Alves, et al.
Birth Defects Research|April 17, 2020
Infantile hypertrophic pyloric stenosis in patients with esophageal atresiaChantal A Ten Kate, Rutger W W Brouwer, Yolande van Bever, et al.
Frontiers in Pediatrics|February 21, 2022
Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing ChallengeErwin Brosens, Nina C J Peters, Kim S van Weelden, et al.
Human Mutation|September 17, 2020
Goldberg-Shprintzen syndrome is determined by the absence, or reduced expression levels, of KIFBPKatherine C MacKenzie, Bianca M de Graaf, Andreas Syrimis, et al.
International Journal of Molecular Sciences|January 11, 2022
Multi-Omics Profiling in Marfan Syndrome: Further Insights into the Molecular Mechanisms Involved in Aortic DiseaseJudith M A Verhagen, Joyce Burger, Jos A Bekkers, et al.
Genome Research|October 5, 2012
Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorderPrzemyslaw Szafranski, Avinash V Dharmadhikari, Erwin Brosens, et al.
European Journal of Pediatrics|March 17, 2016
More than fetal urine: enteral uptake of amniotic fluid as a major predictor for fetal growth during late gestationSoyhan Bagci, Erwin Brosens, Dick Tibboel, et al.
Cancers|February 15, 2022
Identification of Early-Onset Metastasis in SF3B1 Mutated Uveal MelanomaWojtek Drabarek, Job van Riet, Josephine Q N Nguyen, et al.
Plos Genetics|August 6, 2021
Size matters: Large copy number losses in Hirschsprung disease patients reveal genes involved in enteric nervous system developmentLaura E Kuil, Katherine C MacKenzie, Clara S Tang, et al.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
International Journal of Molecular Sciences|November 27, 2021
The Somatic Mutation Paradigm in Congenital Malformations: Hirschsprung Disease as a ModelKatherine C MacKenzie, Rhiana Garritsen, Rajendra K Chauhan, et al.
Gastroenterology|March 31, 2018
Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung DiseaseYunia Sribudiani, Rajendra K Chauhan, Maria M Alves, et al.
Birth Defects Research|April 17, 2020
Infantile hypertrophic pyloric stenosis in patients with esophageal atresiaChantal A Ten Kate, Rutger W W Brouwer, Yolande van Bever, et al.
Frontiers in Pediatrics|February 21, 2022
Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing ChallengeErwin Brosens, Nina C J Peters, Kim S van Weelden, et al.
Human Mutation|September 17, 2020
Goldberg-Shprintzen syndrome is determined by the absence, or reduced expression levels, of KIFBPKatherine C MacKenzie, Bianca M de Graaf, Andreas Syrimis, et al.
International Journal of Molecular Sciences|January 11, 2022
Multi-Omics Profiling in Marfan Syndrome: Further Insights into the Molecular Mechanisms Involved in Aortic DiseaseJudith M A Verhagen, Joyce Burger, Jos A Bekkers, et al.
Genome Research|October 5, 2012
Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorderPrzemyslaw Szafranski, Avinash V Dharmadhikari, Erwin Brosens, et al.
European Journal of Pediatrics|March 17, 2016
More than fetal urine: enteral uptake of amniotic fluid as a major predictor for fetal growth during late gestationSoyhan Bagci, Erwin Brosens, Dick Tibboel, et al.
Cancers|February 15, 2022
Identification of Early-Onset Metastasis in SF3B1 Mutated Uveal MelanomaWojtek Drabarek, Job van Riet, Josephine Q N Nguyen, et al.
Plos Genetics|August 6, 2021
Size matters: Large copy number losses in Hirschsprung disease patients reveal genes involved in enteric nervous system developmentLaura E Kuil, Katherine C MacKenzie, Clara S Tang, et al.
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