Raff R - Search Results

1

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: raff r. 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

2

Mosaic tetrasomy 14pter-q13 due to a supernumerary isodicentric derivate of proximal chromosome 14q.

Eggermann T, Gamerdinger U, Bosse K, Heidrich-Kaul C, Raff R, Meyer E, Heil I, Schüler H, Korsch E, Schwanitz G. Eggermann T, et al. Among authors: raff r. Am J Med Genet A. 2005 Apr 30;134(3):305-8. doi: 10.1002/ajmg.a.30631. Am J Med Genet A. 2005. PMID: 15723300 Review.

3

[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. Klin Padiatr. 1998 Nov-Dec;210(6):400-5. doi: 10.1055/s-2008-1043911. Klin Padiatr. 1998. PMID: 9871895 German.

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. Eur J Pediatr Surg. 2000 Aug;10(4):270-5. doi: 10.1055/s-2008-1072372. Eur J Pediatr Surg. 2000. PMID: 11034519

5

Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new cases.

Eggermann K, Mau UA, Bujdosó G, Koltai E, Engels H, Schubert R, Eggermann T, Raff R, Schwanitz G. Eggermann K, et al. Among authors: raff r. Clin Genet. 2002 Jul;62(1):89-93. doi: 10.1034/j.1399-0004.2002.620113.x. Clin Genet. 2002. PMID: 12123494

6

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: raff r. Ann Genet. 2004 Apr-Jun;47(2):191-7. doi: 10.1016/j.anngen.2004.02.004. Ann Genet. 2004. PMID: 15183753

7

Application of specific cytologic, cytogenetic and molecular-cytogenetic techniques for the characterization of solid tumors.

Schwanitz G, Raff R. Schwanitz G, et al. Among authors: raff r. Rocz Akad Med Bialymst. 2005;50:91-6. Rocz Akad Med Bialymst. 2005. PMID: 16358945 Review.

8

New trends in chromosomal investigation in children with cardiovascular malformations.

Schellberg R, Schwanitz G, Grävinghoff L, Kallenberg R, Trost D, Raff R, Wiebe W. Schellberg R, et al. Among authors: raff r. Cardiol Young. 2004 Dec;14(6):622-9. doi: 10.1017/S1047951104006079. Cardiol Young. 2004. PMID: 15679998

9

[Bardet-Biedl syndrome: aspects of nephro-urology and human genetics].

Brühl P, Schwanitz G, Mallmann R, Müller SC, Raff R. Brühl P, et al. Among authors: raff r. Klin Padiatr. 2001 Jan-Feb;213(1):8-12. doi: 10.1055/s-2001-11265. Klin Padiatr. 2001. PMID: 11225476 German.

10

Maternal uniparental disomy 14 in a 15-year-old boy with normal karyotype and no evidence of precocious puberty.

Aretz S, Raff R, Woelfle J, Zerres K, Esser M, Propping P, Eggermann T. Aretz S, et al. Among authors: raff r. Am J Med Genet A. 2005 Jun 15;135(3):336-8. doi: 10.1002/ajmg.a.30755. Am J Med Genet A. 2005. PMID: 15887281 No abstract available.

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