Schwanitz G - Search Results

1

Familial ovarian dysgerminomas (Swyer syndrome) in females associated with 46 XY-karyotype.

Kempe A, Engels H, Schubert R, Meindl A, van der Ven K, Plath H, Rhiem K, Schwanitz G, Schmutzler RK. Kempe A, et al. Among authors: schwanitz g. Gynecol Endocrinol. 2002 Apr;16(2):107-11. Gynecol Endocrinol. 2002. PMID: 12012620

2

Identification of supernumerary der(20) chromosomes by FISH in three patients.

Viersbach R, Engels H, Schwanitz G. Viersbach R, et al. Among authors: schwanitz g. Am J Med Genet. 1997 Jun 13;70(3):278-83. Am J Med Genet. 1997. PMID: 9188666

3

Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping.

Peschka B, Leygraaf J, Hansmann D, Hansmann M, Schröck E, Ried T, Engels H, Schwanitz G, Schubert R. Peschka B, et al. Among authors: schwanitz g. Prenat Diagn. 1999 Dec;19(12):1143-9. Prenat Diagn. 1999. PMID: 10590433 Review.

4

Combination of hypospadias and maldescended testis as cardinal symptoms in gonosomal chromosome aberrations.

Raff R, Schubert R, Schwanitz G, van der Ven K, Brühl P. Raff R, et al. Among authors: schwanitz g. Eur J Pediatr Surg. 2000 Aug;10(4):270-5. doi: 10.1055/s-2008-1072372. Eur J Pediatr Surg. 2000. PMID: 11034519

5

Unbalanced translocation 8;Y (45,X,dic(Y;8)(q11.23;p23.1)): case report and review of terminal 8p deletions.

Bosse K, Eggermann T, Van der Ven K, Raff R, Engels H, Schwanitz G. Bosse K, et al. Among authors: schwanitz g. Ann Genet. 2004 Apr-Jun;47(2):191-7. doi: 10.1016/j.anngen.2004.02.004. Ann Genet. 2004. PMID: 15183753

6

Sperm analyses, genetic counselling and therapy in an infertile carrier of a supernumerary marker chromosome 15.

Paetzold U, Schwanitz G, Schubert R, van der Ven K, Montag M. Paetzold U, et al. Among authors: schwanitz g. Adv Med Sci. 2006;51:31-5. Adv Med Sci. 2006. PMID: 17357273

7

Molecular-cytogenetic investigations of ten term placentae in cases of prenatally diagnosed mosaicism.

Schubert R, Raff R, Schwanitz G. Schubert R, et al. Among authors: schwanitz g. Prenat Diagn. 1996 Oct;16(10):907-13. doi: 10.1002/(SICI)1097-0223(199610)16:10<907::AID-PD968>3.0.CO;2-Q. Prenat Diagn. 1996. PMID: 8938059

8

Clinical, cytogenetic, and molecular findings in 45,X/47,XX,+18 mosaicism: clinical report and review of the literature.

Schubert R, Eggermann T, Hofstaetter C, von Netzer B, Knöpfle G, Schwanitz G. Schubert R, et al. Among authors: schwanitz g. Am J Med Genet. 2002 Jul 1;110(3):278-82. doi: 10.1002/ajmg.10442. Am J Med Genet. 2002. PMID: 12116238 Review.

9

Report of two new cases of Pallister-Killian syndrome confirmed by FISH: tissue-specific mosaicism and loss of i(12p) by in vitro selection.

Schubert R, Viersbach R, Eggermann T, Hansmann M, Schwanitz G. Schubert R, et al. Among authors: schwanitz g. Am J Med Genet. 1997 Oct 3;72(1):106-10. doi: 10.1002/(sici)1096-8628(19971003)72:1<106::aid-ajmg21>3.0.co;2-u. Am J Med Genet. 1997. PMID: 9295085

10

[Undescended testis and hypospadia in sex chromosomal aberrations].

Raff R, Schubert R, Schwanitz G, van der Ven K, Schweikert HU, Brühl P. Raff R, et al. Among authors: schwanitz g. Klin Padiatr. 1998 Nov-Dec;210(6):400-5. doi: 10.1055/s-2008-1043911. Klin Padiatr. 1998. PMID: 9871895 German.

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