Works matching IS 03406717 AND DT 2021 AND VI 140 AND IP 2
Results: 10
Deciphering the complexity of simple chromosomal insertions by genome sequencing.
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- Human Genetics, 2021, v. 140, n. 2, p. 361, doi. 10.1007/s00439-020-02210-x
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Genetic evidence suggests a sense of family, parity and conquest in the Xiongnu Iron Age nomads of Mongolia.
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- Human Genetics, 2021, v. 140, n. 2, p. 349, doi. 10.1007/s00439-020-02209-4
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Population genetics: past, present, and future.
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- Human Genetics, 2021, v. 140, n. 2, p. 231, doi. 10.1007/s00439-020-02208-5
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Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients.
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- Human Genetics, 2021, v. 140, n. 2, p. 321, doi. 10.1007/s00439-020-02207-6
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Identifying adaptive alleles in the human genome: from selection mapping to functional validation.
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- Human Genetics, 2021, v. 140, n. 2, p. 241, doi. 10.1007/s00439-020-02206-7
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A pooled genome-wide association study identifies pancreatic cancer susceptibility loci on chromosome 19p12 and 19p13.3 in the full-Jewish population.
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- Human Genetics, 2021, v. 140, n. 2, p. 309, doi. 10.1007/s00439-020-02205-8
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- Article
A Southeast Asian origin for present-day non-African human Y chromosomes.
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- Human Genetics, 2021, v. 140, n. 2, p. 299, doi. 10.1007/s00439-020-02204-9
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- Article
Interplay between probe design and test performance: overlap between genomic regions of interest, capture regions and high quality reference calls influence performance of WES-based assays.
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- Human Genetics, 2021, v. 140, n. 2, p. 289, doi. 10.1007/s00439-020-02201-y
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- Article
Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease.
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- Human Genetics, 2021, v. 140, n. 2, p. 333, doi. 10.1007/s00439-020-02200-z
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- Article
Combi-CRISPR: combination of NHEJ and HDR provides efficient and precise plasmid-based knock-ins in mice and rats.
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- Human Genetics, 2021, v. 140, n. 2, p. 277, doi. 10.1007/s00439-020-02198-4
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- Article