Exome sequencing identifies variants in infants with sacral agenesis is a research paper published in Birth Defects Research (2022). On theSindex it has a DataRank of 0. It has been cited 4 times.
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Linked data & code
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ACL HHS
Grant: U01DD001223
NHGRI NIH HHS
Grant: UM1 HG006493
NICHD NIH HHS
Grant: HHSN275201100001I
NCBDD CDC HHS
Grant: U01 DD001226
NICHD NIH HHS
Grant: HHSN275201100001C
NIEHS NIH HHS
Grant: P30 ES010126
NCBDD CDC HHS
Grant: U01 DD001035
NCBDD CDC HHS
Grant: U01 DD001227
NICHD NIH HHS
Grant: HHSN275201100001G
NHGRI NIH HHS
Grant: U24 HG008956
National Institutes of Health
Grant: 5U24HG008956-02
NHGRI Genome Sequencing Program Coordinating Center
National Institutes of Health
Grant: 5U01DD001035-02
Iowa CBDRP: Birth Defects Study To Evaluate Pregnancy exposureS
National Institutes of Health
Grant: 3UM1HG006493-07S2
UW Center for Mendelian Genomics
National Institutes of Health
Grant: 1U01DD001223-01
Iowa CBDRP: Component A BD-STEPS II Core
National Heart, Lung, and Blood Institute
National Institutes of Health
California Department of Public Health
Eunice Kennedy Shriver National Institute of Child Health and Human Development
National Human Genome Research Institute
University of Minnesota
Centers for Disease Control and Prevention
FWCI
0.84
Citation Percentile
0.7%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals