Citation: L. Estrada et al., Fgd1, the Cdc42 guanine nucleotide exchange factor responsible for faciogenital dysplasia, is localized to the subcortical actin cytoskeleton and Golgi membrane, HUM MOL GEN, 10(5), 2001, pp. 485-495
Citation: Dm. Martin et al., CHARGE association with choanal atresia and inner ear hypoplasia in a child with a de novo chromosome translocation t(2;7)(p14;q21.11), AM J MED G, 99(2), 2001, pp. 115-119
Citation: P. Hedera et Jl. Gorski, Retinitis pigmentosa, growth hormone deficiency, and acromelic skeletal dysplasia in two brothers: Possible familial RHYNS syndrome, AM J MED G, 101(2), 2001, pp. 142-145
Citation: Dm. Martin et Jl. Gorski, Ocular malformations, postaxial polydactyly, and delayed intramembranous ossification: a new autosomal dominant condition, J MED GENET, 38(8), 2001, pp. 547-551
Citation: Jl. Gorski et al., Skeletal-specific expression of Fgd1 during bone formation and skeletal defects in Faciogenital Dysplasia (FGDY; Aarskog syndrome), DEV DYNAM, 218(4), 2000, pp. 573-586
Authors:
Pasteris, NG
Nagata, K
Hall, A
Gorski, JL
Citation: Ng. Pasteris et al., Isolation, characterization, and mapping of the mouse Fgd3 gene, a new faciogenital dysplasia (FGD1; Aarskog Syndrome) gene homologue, GENE, 242(1-2), 2000, pp. 237-247
Authors:
Fang, JM
Dagenais, SL
Erickson, RP
Arlt, MF
Glynn, MW
Gorski, JL
Seaver, LH
Glover, TW
Citation: Jm. Fang et al., Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome, AM J HU GEN, 67(6), 2000, pp. 1382-1388
Citation: Ng. Pasteris et Jl. Gorski, Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues, GENOMICS, 60(1), 1999, pp. 57-66