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Roberts syndrome and SC phocomelia. A single genetic entity.
Römke C, Froster-Iskenius U, Heyne K, Höhn W, Hof M, Grzejszczyk G, Rauskolb R, Rehder H, Schwinger E. Römke C, et al. Among authors: rehder h. Clin Genet. 1987 Mar;31(3):170-7. doi: 10.1111/j.1399-0004.1987.tb02790.x. Clin Genet. 1987. PMID: 3568444
Prenatal diagnosis of a 46,XX/47,XX, + 12 mosaic.
Jensen PK, Hahnemann N, Rehder H, Schwinger E, Friedrich U. Jensen PK, et al. Among authors: rehder h. Prenat Diagn. 1984 Jul-Aug;4(4):307-9. doi: 10.1002/pd.1970040411. Prenat Diagn. 1984. PMID: 6483791
Neural tube defects in chromosomally normal and abnormal human embryos.
Coerdt W, Miller K, Holzgreve W, Rauskolb R, Schwinger E, Rehder H. Coerdt W, et al. Among authors: rehder h. Ultrasound Obstet Gynecol. 1997 Dec;10(6):410-5. doi: 10.1046/j.1469-0705.1997.10060410.x. Ultrasound Obstet Gynecol. 1997. PMID: 9476327 Free article.
Neuropathology of Raine syndrome.
Rickert CH, Rieder H, Rehder H, Hülskamp G, Hörnig-Franz I, Louwen F, Paulus W. Rickert CH, et al. Among authors: rehder h. Acta Neuropathol. 2002 Mar;103(3):281-7. doi: 10.1007/s00401-001-0469-5. Epub 2001 Dec 5. Acta Neuropathol. 2002. PMID: 11907809
154 results