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H Lipson

Showing results (91-100 of 99) with videos related to

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American Journal of Human Genetics|October 1, 1994
Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen geneM D Briggs, H Choi, M L Warman, et al.
American Journal of Medical Genetics. Part A|September 3, 2021
Expanding the phenotype: Four new cases and hope for treatment in Bachmann-Bupp syndromeElizabeth A VanSickle, Julianne Michael, André S Bachmann, et al.
Biofabrication|August 24, 2012
Rapid 3D printing of anatomically accurate and mechanically heterogeneous aortic valve hydrogel scaffoldsL A Hockaday, K H Kang, N W Colangelo, et al.
American Journal of Human Genetics|June 19, 1998
Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutationsW A Paznekas, M L Cunningham, T D Howard, et al.
IJTLD Open|November 17, 2025
Diagnostic accuracy of the Cepheid MTB host response assay for the detection of pulmonary TBY Alkabab, Y Rani, M Farhad, et al.
Molecular Genetics and Metabolism|June 5, 2012
Outcome of infants diagnosed with 3-methyl-crotonyl-CoA-carboxylase deficiency by newborn screeningGeorgianne L Arnold, Denise Salazar, Julie A Neidich, et al.
The Journal of Pediatrics|March 6, 2009
Efficacy of sapropterin dihydrochloride in increasing phenylalanine tolerance in children with phenylketonuria: a phase III, randomized, double-blind, placebo-controlled studyFriedrich K Trefz, Barbara K Burton, Nicola Longo, et al.
Human Mutation|January 22, 2008
Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinaseD P Dimmock, Q Zhang, C Dionisi-Vici, et al.
American Journal of Human Genetics|January 15, 2019
Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF PathwayJustyna A Karolak, Marie Vincent, Gail Deutsch, et al.
Pageof 10

Showing results (91-100 of 99) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 99 results.
American Journal of Human Genetics|October 1, 1994
Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen geneM D Briggs, H Choi, M L Warman, et al.
American Journal of Medical Genetics. Part A|September 3, 2021
Expanding the phenotype: Four new cases and hope for treatment in Bachmann-Bupp syndromeElizabeth A VanSickle, Julianne Michael, André S Bachmann, et al.
Biofabrication|August 24, 2012
Rapid 3D printing of anatomically accurate and mechanically heterogeneous aortic valve hydrogel scaffoldsL A Hockaday, K H Kang, N W Colangelo, et al.
American Journal of Human Genetics|June 19, 1998
Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutationsW A Paznekas, M L Cunningham, T D Howard, et al.
IJTLD Open|November 17, 2025
Diagnostic accuracy of the Cepheid MTB host response assay for the detection of pulmonary TBY Alkabab, Y Rani, M Farhad, et al.
Molecular Genetics and Metabolism|June 5, 2012
Outcome of infants diagnosed with 3-methyl-crotonyl-CoA-carboxylase deficiency by newborn screeningGeorgianne L Arnold, Denise Salazar, Julie A Neidich, et al.
The Journal of Pediatrics|March 6, 2009
Efficacy of sapropterin dihydrochloride in increasing phenylalanine tolerance in children with phenylketonuria: a phase III, randomized, double-blind, placebo-controlled studyFriedrich K Trefz, Barbara K Burton, Nicola Longo, et al.
Human Mutation|January 22, 2008
Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinaseD P Dimmock, Q Zhang, C Dionisi-Vici, et al.
American Journal of Human Genetics|January 15, 2019
Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF PathwayJustyna A Karolak, Marie Vincent, Gail Deutsch, et al.
Pageof 10