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Lakshmi Mehta

Showing results (1-10 of 45) with videos related to

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Pediatric Endocrinology Reviews : PER|May 23, 2019
Molecular Genetics of Noonan Syndrome and RASopathiesJun Liao, Lakshmi Mehta
Seminars in Nephrology|July 17, 2017
Hereditary Renal DiseasesLakshmi Mehta, Belinda Jim
Pediatric Endocrinology Reviews : PER|May 23, 2019
Clinical Manifestations of Noonan Syndrome and Related DisordersMargo Sheck Breilyn, Lakshmi Mehta
Endocrinology and Metabolism Clinics of North America|June 1, 2016
Genetic Techniques in the Evaluation of Short StatureChristopher J Romero, Lakshmi Mehta, Robert Rapaport
Journal of Pediatric Genetics|September 15, 2016
17q12 Deletion in a patient with Williams syndrome: Case report and review of the literatureLilian Cohen, Joy Samanich, Quilu Pan, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|December 14, 2011
Mandibular distraction in the setting of chromosome 4q deletionPeter J Taub, Michael Wolfeld, Jessica Cohen-Pfeffer, et al.
American Journal of Medical Genetics. Part A|October 15, 2011
Clinical and molecular characterization of chromosome 7p22.1 microduplication detected by array CGHJacqueline V Chui, James D Weisfeld-Adams, James Tepperberg, et al.
European Journal of Medical Genetics|October 13, 2012
Phenotypic heterogeneity in a family with a small atypical microduplication of chromosome 22q11.2 involving TBX1James D Weisfeld-Adams, Lisa Edelmann, Inder K Gadi, et al.
Molecular Genetics and Metabolism|July 20, 2010
Pompe disease: dramatic improvement in gastrointestinal function following enzyme replacement therapy. A report of three later-onset patientsDonna L Bernstein, Martin G Bialer, Lakshmi Mehta, et al.
Genomics|April 12, 2005
Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genesDeepak Kamnasaran, Chih-Ping Chen, Koenraad Devriendt, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Pediatric Endocrinology Reviews : PER|May 23, 2019
Molecular Genetics of Noonan Syndrome and RASopathiesJun Liao, Lakshmi Mehta
Seminars in Nephrology|July 17, 2017
Hereditary Renal DiseasesLakshmi Mehta, Belinda Jim
Pediatric Endocrinology Reviews : PER|May 23, 2019
Clinical Manifestations of Noonan Syndrome and Related DisordersMargo Sheck Breilyn, Lakshmi Mehta
Endocrinology and Metabolism Clinics of North America|June 1, 2016
Genetic Techniques in the Evaluation of Short StatureChristopher J Romero, Lakshmi Mehta, Robert Rapaport
Journal of Pediatric Genetics|September 15, 2016
17q12 Deletion in a patient with Williams syndrome: Case report and review of the literatureLilian Cohen, Joy Samanich, Quilu Pan, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|December 14, 2011
Mandibular distraction in the setting of chromosome 4q deletionPeter J Taub, Michael Wolfeld, Jessica Cohen-Pfeffer, et al.
American Journal of Medical Genetics. Part A|October 15, 2011
Clinical and molecular characterization of chromosome 7p22.1 microduplication detected by array CGHJacqueline V Chui, James D Weisfeld-Adams, James Tepperberg, et al.
European Journal of Medical Genetics|October 13, 2012
Phenotypic heterogeneity in a family with a small atypical microduplication of chromosome 22q11.2 involving TBX1James D Weisfeld-Adams, Lisa Edelmann, Inder K Gadi, et al.
Molecular Genetics and Metabolism|July 20, 2010
Pompe disease: dramatic improvement in gastrointestinal function following enzyme replacement therapy. A report of three later-onset patientsDonna L Bernstein, Martin G Bialer, Lakshmi Mehta, et al.
Genomics|April 12, 2005
Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genesDeepak Kamnasaran, Chih-Ping Chen, Koenraad Devriendt, et al.
Pageof 5