Lexikalischer Teil
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-55694-4_5
Reference6058 articles.
1. Leber, R.R., M.May, S.Pouls et al., Non-syndromatic X-linked mental retardation associated with a mis- sense mutation (P312L) in the FGD1 gene. Clin. Genet. 61 (2002) 139–145.
2. Porteous, M.E.M., A.Curtis, S.Lindsay et al., The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xpll.2-Xql3). Genomics 14 (1992) 298–301.
3. Teebi, A.S., J.K.Rucquoi and M.S.Meyn, AARSKOG syn-drome: Report of a family and discussion of nosology. Am.J.Med.Genet. 46 (1993) 501–509.
4. Zheng, Y., D J.Fischer, M.F.Santos et al., The faciogenital dysplasia gene product FGD1 functions as a Cdc42Hs-specific guanine-nucleotide exchange factor. J.Biol.Chem. 52 (1996) 33169–33172.
5. D’Avanzo, M., V.Pistoia, R.Santinelli et al. Heterogeneity of the erythropoietic defect in two cases of Aase-Smith syndrome. Pediat.Hematol.Oncol. 11 (1994) 189–195.
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