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Page 1
Prenatal exclusion of choroideremia.
van den Hurk JA, van Zandvoort PM, Brunsmann F, Pawlowitzki IH, Holzgreve W, Szabo P, Cremers FP, van Oost BA. van den Hurk JA, et al. Among authors: brunsmann f. Am J Med Genet. 1992 Dec 1;44(6):822-3. doi: 10.1002/ajmg.1320440621. Am J Med Genet. 1992. PMID: 1362326
Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia.
Cremers FP, van de Pol DJ, Wieringa B, Collins FS, Sankila EM, Siu VM, Flintoff WF, Brunsmann F, Blonden LA, Ropers HH. Cremers FP, et al. Among authors: brunsmann f. Proc Natl Acad Sci U S A. 1989 Oct;86(19):7510-4. doi: 10.1073/pnas.86.19.7510. Proc Natl Acad Sci U S A. 1989. PMID: 2798422 Free PMC article.
Choroideremia-locus maps between DXS3 and DXS11 on Xq.
Gal A, Brunsmann F, Hogenkamp D, Rüther K, Ahlert D, Wienker TF, Hammerstein W, Pawlowitzki IH. Gal A, et al. Among authors: brunsmann f. Hum Genet. 1986 Jun;73(2):123-6. doi: 10.1007/BF00291600. Hum Genet. 1986. PMID: 3755117
Acceptability of prenatal diagnosis for retinitis pigmentosa.
Pawlowitzki IH, Rüther K, Brunsmann F, von Gizycki R. Pawlowitzki IH, et al. Among authors: brunsmann f. Lancet. 1986 Dec 13;2(8520):1394-5. doi: 10.1016/s0140-6736(86)92033-7. Lancet. 1986. PMID: 2878250 No abstract available.
[Development of disease-specific patient groups within Pro Retina].
von Gizycki R, Brunsmann F, Rybalko A, Hildebrandt AG, Rüther K. von Gizycki R, et al. Among authors: brunsmann f. Ophthalmologe. 2009 Jul;106(7):639-45. doi: 10.1007/s00347-009-1990-5. Ophthalmologe. 2009. PMID: 19572133 Review. German.
27 results