TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci is a research paper published in Human Molecular Genetics (2020). On theSindex it has a DataRank of 0. It has been cited 22 times.
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National Institutes of Health
Grant: K23HD077043
National Institutes of Health
Grant: P50HD028138
NICHD NIH HHS
Grant: R01 HD096324
National Institutes of Health
Grant: 5K23HD077043-03
Biologic Roles of Novel Axonal Guidance Genes in Isolated GnRH Deficiency
National Institutes of Health
Grant: 5P50HD028138-28
Harvard Reproductive Endocrine Sciences Center
FWCI
1.28
Citation Percentile
0.8%
Citation Trend
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