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51. A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort

52. Healthcare Utilization and Patients’ Perspectives After Receiving a Positive Genetic Test for Familial Hypercholesterolemia

56. A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort

60. Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate

62. Design and Implementation of a Randomized Controlled Trial of Genomic Counseling for Patients with Chronic Disease

63. Dominant-negative variants in CBX1cause a neurodevelopmental disorder

65. Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder

66. Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate.

68. Response to the letter by Collins and Schimke

71. Proceedings from the 9th annual conference on the science of dissemination and implementation: Washington, DC, USA. 14-15 December 2016

72. Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder.

73. Healthcare Utilization and Patients’ Perspectives After Receiving a Positive Genetic Test for Familial Hypercholesterolemia: A Pilot Study.

74. eP420 - Evaluating the mutational spectrum of SIN3A alterations: a case series of patients profiled by next generation sequencing.

75. eP193 - ClinGen's actionability working groups: development and early implementation of an assertion rubric for clinical actionability.

76. OP097 - Clinical actionability of secondary findings in the pediatric context.

77. eP010 - Utility of specific amino acid ratios in screening for pyruvate dehydrogenase complex deficiencies and other disorders associated with lactic acidosis.

78. Inherited and de novo variants extend the etiology of TAOK1 -associated neurodevelopmental disorder.

79. De novo loss-of-function variants in NSD2 ( WHSC1 ) associate with a subset of Wolf-Hirschhorn syndrome.

80. The Pharmacogenomics Research Network Translational Pharmacogenetics Program: overcoming challenges of real-world implementation.

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