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Paul R Mark

Showing results (1-10 of 30) with videos related to

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American Journal of Medical Genetics. Part A|April 29, 2022
NAD+ deficiency in human congenital malformations and miscarriage: A new model of pleiotropyPaul R Mark
Journal of Colloid and Interface Science|December 23, 2011
Understanding nanoparticle assembly: a simulation approach to SERS-active dimersPaul R Mark, Laura Fabris
European Journal of Medical Genetics|February 14, 2015
Comment on critical region for talipes equinovarus in patients with 5q23 deletionsMaria Tecos, Paul R Mark
American Journal of Medical Genetics. Part A|September 18, 2020
Lethal renal anomalies in a fetus with 21q22.11-q22.12 deletionKathleen Dinh, Paul R Mark
Birth Defects Research|December 1, 2022
Viewing teratogens through the lens of nicotinamide adenine dinucleotide (NAD+)Paul R Mark, Sally L Dunwoodie
Cardiology in the Young|March 5, 2021
Two cases of different genetic variants of alveolar capillary dysplasia associated with left-sided obstructive CHDsJosue Diaz-Frias, Paul R Mark, E Oliver Aregullin
American Journal of Medical Genetics. Part A|January 5, 2011
Association of a p.Pro786Leu variant in COL2A1 with mild spondyloepiphyseal dysplasia congenita in a three-generation familyPaul R Mark, Wilfredo Torres-Martinez, Ralph S Lachman, et al.
Cold Spring Harbor Molecular Case Studies|July 15, 2020
SLC6A1 G443D associated with developmental delay and epilepsySeth Devries, Monica Mulder, Jacob G Charron, et al.
American Journal of Medical Genetics. Part A|December 25, 2018
Clinical spectrum of BCS1L Mitopathies and their underlying structural relationshipsRachael A Baker, Jessica R C Priestley, Amy M Wilstermann, et al.
Biorxiv : the Preprint Server for Biology|January 20, 2025
A zebrafish model of nicotinamide adenine dinucleotide (NAD<sup>+</sup>) deficiency-derived congenital disordersVisakuo Tsurho, Carla Gilliland, Jessica Ensing, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|April 29, 2022
NAD+ deficiency in human congenital malformations and miscarriage: A new model of pleiotropyPaul R Mark
Journal of Colloid and Interface Science|December 23, 2011
Understanding nanoparticle assembly: a simulation approach to SERS-active dimersPaul R Mark, Laura Fabris
European Journal of Medical Genetics|February 14, 2015
Comment on critical region for talipes equinovarus in patients with 5q23 deletionsMaria Tecos, Paul R Mark
American Journal of Medical Genetics. Part A|September 18, 2020
Lethal renal anomalies in a fetus with 21q22.11-q22.12 deletionKathleen Dinh, Paul R Mark
Birth Defects Research|December 1, 2022
Viewing teratogens through the lens of nicotinamide adenine dinucleotide (NAD+)Paul R Mark, Sally L Dunwoodie
Cardiology in the Young|March 5, 2021
Two cases of different genetic variants of alveolar capillary dysplasia associated with left-sided obstructive CHDsJosue Diaz-Frias, Paul R Mark, E Oliver Aregullin
American Journal of Medical Genetics. Part A|January 5, 2011
Association of a p.Pro786Leu variant in COL2A1 with mild spondyloepiphyseal dysplasia congenita in a three-generation familyPaul R Mark, Wilfredo Torres-Martinez, Ralph S Lachman, et al.
Cold Spring Harbor Molecular Case Studies|July 15, 2020
SLC6A1 G443D associated with developmental delay and epilepsySeth Devries, Monica Mulder, Jacob G Charron, et al.
American Journal of Medical Genetics. Part A|December 25, 2018
Clinical spectrum of BCS1L Mitopathies and their underlying structural relationshipsRachael A Baker, Jessica R C Priestley, Amy M Wilstermann, et al.
Biorxiv : the Preprint Server for Biology|January 20, 2025
A zebrafish model of nicotinamide adenine dinucleotide (NAD<sup>+</sup>) deficiency-derived congenital disordersVisakuo Tsurho, Carla Gilliland, Jessica Ensing, et al.
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