Zain Bassam Mohammad DARDAS to Phenotype
This is a "connection" page, showing publications Zain Bassam Mohammad DARDAS has written about Phenotype.
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NODAL variants are associated with a continuum of laterality defects from simple D-transposition of the great arteries to heterotaxy. Genome Med. 2024 04 03; 16(1):53.
Score: 0.102
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TBX5 variant with the novel phenotype of mixed-type total anomalous pulmonary venous return in Holt-Oram Syndrome and variable intrafamilial heart defects. Mol Med Rep. 2022 06; 25(6).
Score: 0.022
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Clinical heterogeneity in retinitis pigmentosa caused by variants in RP1 and RLBP1 in five extended consanguineous pedigrees. Mol Vis. 2020; 26:445-458.
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Extending the spectrum of CLRN1- and ABCA4-associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing. Mol Genet Genomic Med. 2020 03; 8(3):e1123.
Score: 0.019
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Novel CERKL variant in consanguineous Jordanian pedigrees with inherited retinal dystrophies. Can J Ophthalmol. 2019 02; 54(1):51-59.
Score: 0.017