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2. Segregation analyses and a genome-wide linkage search confirm genetic heterogeneity and suggest oligogenic inheritance in some Milroy congenital primary lymphedema families;Holberg;Am J Med Genet,2000
3. Sex-limited penetrance of lymphedema to females with CELSR1 haploinsufficiency: a second family;Erickson;Clin Genet,2019
4. From childhood onset lymphedema to fatal fetal hydrops: possible modifying genes for a FOXC2 mutation;Lai;Lymphology,2018
5. Non-contrast MR lymphography of rare lymphatic abnormalities;Seckeler;Lymphology,2020