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For: Hausman-Kedem M, Ben-Sira L, Kidron D, Ben-Shachar S, Straussberg R, Marom D, Ponger P, Bar-Shira A, Malinger G, Fattal-Valevski A. Deletion in COL4A2 is associated with a three-generation variable phenotype: from fetal to adult manifestations. Eur J Hum Genet 2021. [PMID: 33837277 DOI: 10.1038/s41431-021-00880-3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Mao M, Labelle-Dumais C, Tufa SF, Keene DR, Gould DB. Elevated TGFβ signaling contributes to ocular anterior segment dysgenesis in Col4a1 mutant mice. Matrix Biol 2022:S0945-053X(22)00066-X. [PMID: 35525525 DOI: 10.1016/j.matbio.2022.05.001] [Reference Citation Analysis]
2 McNeill A. Genotyping arrays, population genetic studies and clinical implications. Eur J Hum Genet 2021;29:1591-2. [PMID: 34616014 DOI: 10.1038/s41431-021-00979-7] [Reference Citation Analysis]