Publisher
Springer Science and Business Media LLC
Subject
Biochemistry (medical),Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry
Reference23 articles.
1. Hasi-Zogaj M, Sebold C, Heard P, Carter E, Soileau B, Hill A, Rupert D, Perry B, Atkinson S, O’Donnell L, Gelfond J, Lancaster J, Fox PT, Hale DE, Cody JD. A review of 18p deletions. Am J Med Genet C Semin Med Genet. 2015;169:251–64.
2. Taine L, Goizet C, Wen ZQ, Chateil JF, Battin J, Saura R, Lacombe D. 18p monosomy with midline defects and a de novo satellite identified by FISH. Ann Genet. 1997;40:158–63.
3. Tonk V, Krishna J. Case report: denovo inherited 18p deletion in a mother-fetus pair with extremely variable expression, confirmed by fluorescence in situ hybridization (FISH) analysis. Eur J Obstet Gynecol Reprod Biol. 1997;73:193–6.
4. Artman HG, Morris CA, Stock AD. 18p- syndrome and hypopituitarism. J Med Genet. 1992;29:671–2.
5. Portnoï MF, Gruchy N, Marlin S, Finkel L, Denoyelle F, Dubourg C, Odent S, Siffroi JP, Le Bouc Y, Houang M. Midline defects in deletion 18p syndrome: clinical and molecular characterization of three patients. Clin Dysmorphol. 2007;16:247–52.
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