Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM007748-08
Application #
3537815
Study Section
Genetic Basis of Disease Review Committee (GBD)
Project Start
1979-07-01
Project End
1989-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
8
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Harvard University
Department
Type
Schools of Medicine
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
Stachler, Matthew D; Camarda, Nicholas D; Deitrick, Christopher et al. (2018) Detection of Mutations in Barrett's Esophagus Before Progression to High-Grade Dysplasia or Adenocarcinoma. Gastroenterology 155:156-167
Srivastava, Siddharth; Desai, Sonal; Cohen, Julie et al. (2018) Monogenic disorders that mimic the phenotype of Rett syndrome. Neurogenetics 19:41-47
Wojcik, Monica H; Brodsky, Dara; Stewart, Jane E et al. (2018) Peri-mortem evaluation of infants who die without a diagnosis: focus on advances in genomic technology. J Perinatol 38:1125-1134
Guissart, Claire; Latypova, Xenia; Rollier, Paul et al. (2018) Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia. Am J Hum Genet 102:744-759
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