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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2018 | 3 |
2019 | 1 |
2024 | 0 |
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Page 1
Neu-Laxova syndrome presenting prenatally with increased nuchal translucency and cystic hygroma: The utility of exome sequencing in deciphering the diagnosis.
Am J Med Genet A. 2019 May;179(5):813-816. doi: 10.1002/ajmg.a.61076. Epub 2019 Mar 5.
Am J Med Genet A. 2019.
PMID: 30838783
Clinical and genetic heterogeneity in Dubowitz syndrome: Implications for diagnosis, management and further research.
Innes AM, McInnes BL, Dyment DA.
Innes AM, et al.
Am J Med Genet C Semin Med Genet. 2018 Dec;178(4):387-397. doi: 10.1002/ajmg.c.31661.
Am J Med Genet C Semin Med Genet. 2018.
PMID: 30580484
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The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®.
Hartley T, Balcı TB, Rojas SK, Eaton A, Canada CR, Dyment DA, Boycott KM.
Hartley T, et al.
Am J Med Genet C Semin Med Genet. 2018 Dec;178(4):458-463. doi: 10.1002/ajmg.c.31662.
Am J Med Genet C Semin Med Genet. 2018.
PMID: 30580481
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Genomic evaluation of feed efficiency component traits in Duroc pigs using 80K, 650K and whole-genome sequence variants.
Zhang C, Kemp RA, Stothard P, Wang Z, Boddicker N, Krivushin K, Dekkers J, Plastow G.
Zhang C, et al.
Genet Sel Evol. 2018 Apr 6;50(1):14. doi: 10.1186/s12711-018-0387-9.
Genet Sel Evol. 2018.
PMID: 29625549
Free PMC article.
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