Associated Papers
Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia.
Chen L et al.
Translational Psychiatry, 2024
38951484 (PubMed )
Supplement: 41398_2024_2984_MOESM1_ESM.pdf
Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of SPRY1 (sprouty homolog 1) function.
Tooze RS et al.
Journal of Medical Genetics, 2023
36543535 (PubMed )
Supplement: jmg-2022-108946supp001.pdf
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