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Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism.
Salmonella typhimurium
Disruption of the csk gene, encoding a negative regulator of Src family tyrosine kinases, leads to neural tube defects and embryonic lethality in mice.
Signatures of replication timing, recombination, and sex in the spectrum of rare variants on the human X chromosome and autosomes.
X-chromosome threshold models of bipolar manic-depressive illness.
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X-chromosome threshold models of bipolar manic-depressive illness.
X-chromosome threshold models of bipolar manic-depressive illness. J Psychiatr Res. 1979; 15(4):215-38.
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PubMed
subject areas
Bipolar Disorder
Female
Genotype
Humans
Male
Models, Genetic
Sex Chromosomes
X Chromosome
authors with profiles
Elliot S. Gershon