Associated Papers
Identification of potential causal variants for premature ovarian failure by whole exome sequencing.
Jin H et al.
Bmc Medical Genomics, 2020
ATR-16 syndrome: mechanisms linking monosomy to phenotype.
Babbs C et al.
Journal of Medical Genetics, 2020
32005695 (PubMed )
Supplement: jmedgenet-2019-106528supp001.pdf
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