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Kim L McBride

Showing results (1-10 of 116) with videos related to

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Expert Review of Endocrinology & Metabolism|February 13, 2019
Idursulfase: enzyme replacement therapy for mucopolysaccharidosis Type II (Hunter syndrome)Kim L McBride
American Journal of Medical Genetics. Part A|July 9, 2011
Rebuttal to the invited comment of Opitz and CareyKim L McBride
American Journal of Medical Genetics. Part A|December 15, 2012
Severe hypertrophic cardiomyopathy in Noonan syndrome-consider sequencing genes encoding sarcomeric proteinsKim L McBride
The New England Journal of Medicine|May 23, 2003
Case 27-2002: late-onset infantile neuronal ceroid lipofuscinosisKim L McBride
Heart (British Cardiac Society)|April 5, 2011
Heredity of bicuspid aortic valve: is family screening indicated?Kim L McBride, Vidu Garg
Annals of the New York Academy of Sciences|October 21, 2010
Impact of Mendelian inheritance in cardiovascular diseaseKim L McBride, Vidu Garg
Circulation. Cardiovascular Genetics|October 14, 2017
Modifying Mendel Redux: Unbiased Approaches Can Find ModifiersKim L McBride, Stephanie M Ware
Seminars in Pediatric Neurology|April 24, 2021
Update in the MucopolysaccharidosesKim L McBride, Kevin M Flanigan
Molecular Genetics and Metabolism|September 7, 2012
Cardiac teratogenicity in mouse maternal phenylketonuria: defining phenotype parameters and genetic background influencesNikki J Seagraves, Kim L McBride
Circulation. Cardiovascular Genetics|June 21, 2012
Modifying Mendel: approaches for identification of susceptibility alleles for human cardiovascular malformationsKim L McBride, Stephanie M Ware
Pageof 12

Showing results (1-10 of 116) with videos related to

Sort By:
Pageof 12
Expert Review of Endocrinology & Metabolism|February 13, 2019
Idursulfase: enzyme replacement therapy for mucopolysaccharidosis Type II (Hunter syndrome)Kim L McBride
American Journal of Medical Genetics. Part A|July 9, 2011
Rebuttal to the invited comment of Opitz and CareyKim L McBride
American Journal of Medical Genetics. Part A|December 15, 2012
Severe hypertrophic cardiomyopathy in Noonan syndrome-consider sequencing genes encoding sarcomeric proteinsKim L McBride
The New England Journal of Medicine|May 23, 2003
Case 27-2002: late-onset infantile neuronal ceroid lipofuscinosisKim L McBride
Heart (British Cardiac Society)|April 5, 2011
Heredity of bicuspid aortic valve: is family screening indicated?Kim L McBride, Vidu Garg
Annals of the New York Academy of Sciences|October 21, 2010
Impact of Mendelian inheritance in cardiovascular diseaseKim L McBride, Vidu Garg
Circulation. Cardiovascular Genetics|October 14, 2017
Modifying Mendel Redux: Unbiased Approaches Can Find ModifiersKim L McBride, Stephanie M Ware
Seminars in Pediatric Neurology|April 24, 2021
Update in the MucopolysaccharidosesKim L McBride, Kevin M Flanigan
Molecular Genetics and Metabolism|September 7, 2012
Cardiac teratogenicity in mouse maternal phenylketonuria: defining phenotype parameters and genetic background influencesNikki J Seagraves, Kim L McBride
Circulation. Cardiovascular Genetics|June 21, 2012
Modifying Mendel: approaches for identification of susceptibility alleles for human cardiovascular malformationsKim L McBride, Stephanie M Ware
Pageof 12