Stengel-Rutkowski S - Search Results

1

45,X constitution in a H-Y antigen positive boy with partial monosomy 5p.

Seidel H, Miller K, Spoljar M, Stengel-Rutkowski S. Seidel H, et al. Clin Genet. 1981 Apr;19(4):290-7. doi: 10.1111/j.1399-0004.1981.tb00711.x. Clin Genet. 1981. PMID: 7273470 No abstract available.

2

[Transexuality and X-Y antigen (author's transl)].

Eicher W, Spoljar M, Richter K, Cleve H, Murken JD, Stengel-Rutkowski S, Steindl E. Eicher W, et al. Geburtshilfe Frauenheilkd. 1980 Jun;40(6):529-40. doi: 10.1055/s-2008-1037371. Geburtshilfe Frauenheilkd. 1980. PMID: 7409418 German.

3

[Transsexualism and the H-Y antigen].

Eicher W, Spoljar M, Murken JD, Richter K, Cleve H, Stengel-Rutkowski S. Eicher W, et al. Fortschr Med. 1981 Jan 15;99(1-2):9-12. Fortschr Med. 1981. PMID: 7203339 German.

4

Familial Wolf's syndrome with a hidden 4p deletion by translocation of an 8p segment. Unbalanced inheritance from a maternal translocation (4;8)(p15.3;p22). Case report, review and risk estimates.

Stengel-Rutkowski S, Warkotsch A, Schimanek P, Stene J. Stengel-Rutkowski S, et al. Clin Genet. 1984 Jun;25(6):500-21. doi: 10.1111/j.1399-0004.1984.tb00494.x. Clin Genet. 1984. PMID: 6539659

5

The dermatoglyphic pattern of the trisomy 9p syndrome.

Rodewald A, Stengel-Rutkowski S, Zankl M. Rodewald A, et al. Clin Genet. 1979 Dec;16(6):405-17. doi: 10.1111/j.1399-0004.1979.tb01349.x. Clin Genet. 1979. PMID: 527248

6

The dermatoglyphic pattern of the trisomy 10p syndrome.

Rodewald A, Stengel-Rutkowski S. Rodewald A, et al. Clin Genet. 1978 Dec;14(6):330-7. doi: 10.1111/j.1399-0004.1978.tb02098.x. Clin Genet. 1978. PMID: 729197

7

Partial trisomy 8q. Two case reports with maternal translocation and inverted insertion: phenotype analyses and reflections on the risk.

Stengel-Rutkowski S, Lohse K, Herzog C, Apacik C, Couturier J, Albert A, Belohradsky B. Stengel-Rutkowski S, et al. Clin Genet. 1992 Oct;42(4):178-85. doi: 10.1111/j.1399-0004.1992.tb03234.x. Clin Genet. 1992. PMID: 1424241 Review.

8

Two brothers with multiple congenital anomalies and mental retardation due to disomy (X)(q12-->q13.3) inherited from the mother.

Apacik C, Cohen M, Jakobeit M, Schmucker B, Schuffenhauer S, Thurn und Taxis E, Genzel-Boroviczeny O, Stengel-Rutkowski S. Apacik C, et al. Among authors: stengel rutkowski s. Clin Genet. 1996 Aug;50(2):63-73. doi: 10.1111/j.1399-0004.1996.tb02350.x. Clin Genet. 1996. PMID: 8937763 Review.

9

Aspermia, associated with a presumably balanced X/autosomal translocation karyotype 46, Y, t (X;5) (q28;q11).

Stengel-Rutkowski S, Zankl H, Rodewald A, Scharrer S, Chaudhuri JP, Zang KD. Stengel-Rutkowski S, et al. Hum Genet. 1976 Jan 28;31(1):97-106. doi: 10.1007/BF00270405. Hum Genet. 1976. PMID: 1248827

10

Ambras syndrome: delineation of a unique hypertrichosis universalis congenita and association with a balanced pericentric inversion (8) (p11.2; q22).

Baumeister FA, Egger J, Schildhauer MT, Stengel-Rutkowski S. Baumeister FA, et al. Clin Genet. 1993 Sep;44(3):121-8. doi: 10.1111/j.1399-0004.1993.tb03862.x. Clin Genet. 1993. PMID: 8275569 Review.

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