Brude E - Search Results

1

Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH.

Liehr T, Starke H, Beensen V, Kähler C, Harbich M, Brude E, Ziegler M, Claussen U. Liehr T, et al. Among authors: brude e. Int J Mol Med. 1999 Jan;3(1):11-4. doi: 10.3892/ijmm.3.1.11. Int J Mol Med. 1999. PMID: 9864379

2

Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15--case report plus review of similar cases.

Liehr T, Brude E, Gillessen-Kaesbach G, König R, Mrasek K, von Eggeling F, Starke H. Liehr T, et al. Among authors: brude e. Eur J Med Genet. 2005 Apr-Jun;48(2):175-81. doi: 10.1016/j.ejmg.2005.01.004. Epub 2005 Feb 17. Eur J Med Genet. 2005. PMID: 16053909 Review.

3

[Hypomelanosis Ito in translocation trisomy 9/mosaicism (46,XX/46,XX,t(9;9)(p24;p24)). Spontaneous remission in childhood].

Dereser-Dennl M, Brude E, König R. Dereser-Dennl M, et al. Among authors: brude e. Hautarzt. 2000 Sep;51(9):688-92. doi: 10.1007/s001050051197. Hautarzt. 2000. PMID: 11057398 German.

4

Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS).

Kohlschmidt N, Zielinski J, Brude E, Schäfer D, Olert J, Hallermann C, Coerdt W, Arnemann J. Kohlschmidt N, et al. Among authors: brude e. Prenat Diagn. 2000 Feb;20(2):152-5. doi: 10.1002/(sici)1097-0223(200002)20:2<152::aid-pd738>3.0.co;2-p. Prenat Diagn. 2000. PMID: 10694689

5

Society must decide about prenatal diagnosis.

Schäfer D, Arnemann J, Brude E, Baumann R. Schäfer D, et al. Among authors: brude e. Hum Reprod. 1995 Apr;10(4):768-9. doi: 10.1093/oxfordjournals.humrep.a136035. Hum Reprod. 1995. PMID: 7650118 No abstract available.

6

Detection of TSPY protein in a unilateral microscopic gonadoblastoma of a Turner mosaic patient with a Y-derived marker chromosome.

Hildenbrand R, Schröder W, Brude E, Schepler A, König R, Stutte HJ, Arnemann J. Hildenbrand R, et al. Among authors: brude e. J Pathol. 1999 Dec;189(4):623-6. doi: 10.1002/(SICI)1096-9896(199912)189:4<623::AID-PATH475>3.0.CO;2-#. J Pathol. 1999. PMID: 10629567

7

Distribution of marker-Y chromosome containing cells in different tissues of a Turner mosaic patient with mixed gonadal dysgenesis.

Petrusevska R, Beudt U, Schäfer D, Schneider M, Brude E, Leitner C, Heller K, Arnemann J. Petrusevska R, et al. Among authors: brude e. Clin Genet. 1996 May;49(5):261-6. doi: 10.1111/j.1399-0004.1996.tb03784.x. Clin Genet. 1996. PMID: 8832135

8

Inhibition of osteosarcoma cell proliferation by the Hedgehog-inhibitor cyclopamine.

Warzecha J, Göttig S, Chow KU, Brüning C, Percic D, Boehrer S, Brude E, Kurth A. Warzecha J, et al. Among authors: brude e. J Chemother. 2007 Oct;19(5):554-61. doi: 10.1179/joc.2007.19.5.554. J Chemother. 2007. PMID: 18073155

9

Ocular osteogenesis imperfecta.

Brude E. Brude E. Clin Genet. 1986 Feb;29(2):187. doi: 10.1111/j.1399-0004.1986.tb01251.x. Clin Genet. 1986. PMID: 3955877 No abstract available.

10

Pierre Robin sequence and hyperphalangy--a genetic entity (Catel-Manzke syndrome).

Brude E. Brude E. Eur J Pediatr. 1984 Aug;142(3):222-3. doi: 10.1007/BF00442455. Eur J Pediatr. 1984. PMID: 6540680

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