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P Suzanne Hart

Showing results (11-20 of 32) with videos related to

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Molecular Genetics & Genomic Medicine|July 19, 2017
Medical genetics and genomic medicine in the United States of America. Part 1: history, demographics, legislation, and burden of diseaseCarlos R Ferreira, Debra S Regier, Donald W Hadley, et al.
Pediatric Nephrology (Berlin, Germany)|February 13, 2010
Childhood course of renal insufficiency in a family with a uromodulin gene mutationPéter Schäffer, Eva Gombos, Krisztina Meichelbeck, et al.
The Journal of Biological Chemistry|May 19, 2007
Germ line gain of function with SOS1 mutation in hereditary gingival fibromatosisShyh-Ing Jang, Eun-Jin Lee, P Suzanne Hart, et al.
European Journal of Oral Sciences|July 31, 2003
Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfectaP Suzanne Hart, J Timothy Wright, Mathew Savage, et al.
Cells, Tissues, Organs|May 21, 2011
Amelogenesis imperfecta: genotype-phenotype studies in 71 familiesJ Timothy Wright, Melody Torain, Kimberly Long, et al.
Archives of Oral Biology|May 17, 2005
Variation in dental and skeletal open bite malocclusion in humans with amelogenesis imperfectaDarren B Ravassipour, Cynthia M Powell, Ceib L Phillips, et al.
Human Mutation|June 4, 2008
A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP geneDianalee A McKnight, P Suzanne Hart, Thomas C Hart, et al.
Head & Face Medicine|February 3, 2007
Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfectaMaria C L G Santos, P Suzanne Hart, Mukundhan Ramaswami, et al.
Journal of Periodontology|December 8, 2005
Clinical, genetic, and biochemical findings in two siblings with Papillon-Lefèvre SyndromeN Arzu Cagli, Sema S Hakki, Recep Dursun, et al.
JIMD Reports|February 23, 2013
Noncompaction of the ventricular myocardium and hydrops fetalis in cobalamin C diseasePranoot Tanpaiboon, Jennifer L Sloan, Patrick F Callahan, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Molecular Genetics & Genomic Medicine|July 19, 2017
Medical genetics and genomic medicine in the United States of America. Part 1: history, demographics, legislation, and burden of diseaseCarlos R Ferreira, Debra S Regier, Donald W Hadley, et al.
Pediatric Nephrology (Berlin, Germany)|February 13, 2010
Childhood course of renal insufficiency in a family with a uromodulin gene mutationPéter Schäffer, Eva Gombos, Krisztina Meichelbeck, et al.
The Journal of Biological Chemistry|May 19, 2007
Germ line gain of function with SOS1 mutation in hereditary gingival fibromatosisShyh-Ing Jang, Eun-Jin Lee, P Suzanne Hart, et al.
European Journal of Oral Sciences|July 31, 2003
Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfectaP Suzanne Hart, J Timothy Wright, Mathew Savage, et al.
Cells, Tissues, Organs|May 21, 2011
Amelogenesis imperfecta: genotype-phenotype studies in 71 familiesJ Timothy Wright, Melody Torain, Kimberly Long, et al.
Archives of Oral Biology|May 17, 2005
Variation in dental and skeletal open bite malocclusion in humans with amelogenesis imperfectaDarren B Ravassipour, Cynthia M Powell, Ceib L Phillips, et al.
Human Mutation|June 4, 2008
A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP geneDianalee A McKnight, P Suzanne Hart, Thomas C Hart, et al.
Head & Face Medicine|February 3, 2007
Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfectaMaria C L G Santos, P Suzanne Hart, Mukundhan Ramaswami, et al.
Journal of Periodontology|December 8, 2005
Clinical, genetic, and biochemical findings in two siblings with Papillon-Lefèvre SyndromeN Arzu Cagli, Sema S Hakki, Recep Dursun, et al.
JIMD Reports|February 23, 2013
Noncompaction of the ventricular myocardium and hydrops fetalis in cobalamin C diseasePranoot Tanpaiboon, Jennifer L Sloan, Patrick F Callahan, et al.
Pageof 4