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2 results for author:"Pappas J.G." in Literature citations

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A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.

Bicknell L.S., Farrington-Rock C., Shafeghati Y., Rump P., Alanay Y., Alembik Y., Al-Madani N., Firth H., Karimi-Nejad M.H., Kim C.A. et al.

J. Med. Genet. 44:89-98(2007) · UniProtKB (1) · Mapped (2)

DAX1 mutations map to putative structural domains in a deduced three-dimensional model.

Zhang Y.-H., Guo W., Wagner R.L., Huang B.-L., McCabe L.L., Vilain E., Burris T.P., Anyane-Yeboa K., Burghes A.H.M., Chitayat D. et al.

Am. J. Hum. Genet. 62:855-864(1998) · UniProtKB (1)

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