Grote W - Search Results

1

Interphase cytogenetics on paraffin sections of paediatric extragonadal yolk sac tumours.

Jenderny J, Köster E, Borchers O, Meyer A, Grote W, Harms D, Jänig U. Jenderny J, et al. Among authors: grote w. Virchows Arch. 1996 Apr;428(1):53-7. doi: 10.1007/BF00192927. Virchows Arch. 1996. PMID: 8646370 Review.

2

Detection of chromosome aberrations in paraffin sections of seven gonadal yolk sac tumors of childhood.

Jenderny J, Köster E, Meyer A, Borchers O, Grote W, Harms D, Jänig U. Jenderny J, et al. Among authors: grote w. Hum Genet. 1995 Dec;96(6):644-50. doi: 10.1007/BF00210292. Hum Genet. 1995. PMID: 8522320

3

Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotype.

Jenderny J, Caliebe A, Beyer C, Grote W. Jenderny J, et al. Among authors: grote w. J Med Genet. 1993 Nov;30(11):964-5. doi: 10.1136/jmg.30.11.964. J Med Genet. 1993. PMID: 8301656 Free PMC article.

4

Translocation t(2;5) is not a primary event in Hodgkin's disease. Simultaneous immunophenotyping and interphase cytogenetics.

Weber-Matthiesen K, Deerberg-Wittram J, Rosenwald A, Poetsch M, Grote W, Schlegelberger B. Weber-Matthiesen K, et al. Among authors: grote w. Am J Pathol. 1996 Aug;149(2):463-8. Am J Pathol. 1996. PMID: 8701985 Free PMC article.

5

Interphase cytogenetics of hematological neoplasms under the perspective of the novel WHO classification.

Martín-Subero JI, Gesk S, Harder L, Grote W, Siebert R. Martín-Subero JI, et al. Among authors: grote w. Anticancer Res. 2003 Mar-Apr;23(2A):1139-48. Anticancer Res. 2003. PMID: 12820362 Review.

6

Clarification of dubious karyotypes in Hodgkin's disease by simultaneous fluorescence immunophenotyping and interphase cytogenetics (FICTION).

Weber-Matthiesen K, Deerberg J, Poetsch M, Grote W, Schlegelberger B. Weber-Matthiesen K, et al. Among authors: grote w. Cytogenet Cell Genet. 1995;70(3-4):243-5. doi: 10.1159/000134043. Cytogenet Cell Genet. 1995. PMID: 7789181

7

[Embryonal malformation following etretinate therapy of Darier's disease in the mother].

Kietzmann H, Schwarze I, Grote W, Ravens U, Jänig U, Harms D. Kietzmann H, et al. Among authors: grote w. Dtsch Med Wochenschr. 1986 Jan 10;111(2):60-2. doi: 10.1055/s-2008-1068402. Dtsch Med Wochenschr. 1986. PMID: 3940838 German.

8

Malformation of fetus conceived 4 months after termination of maternal etretinate treatment.

Grote W, Harms D, Jänig U, Kietzmann H, Ravens U, Schwarze I. Grote W, et al. Lancet. 1985 Jun 1;1(8440):1276. doi: 10.1016/s0140-6736(85)92344-x. Lancet. 1985. PMID: 2860474 No abstract available.

9

Prenatal diagnosis of a short-rib-polydactylia syndrome type Saldino-Noonan at 17 weeks' gestation.

Grote W, Weisner D, Jänig U, Harms D, Wiedemann HR. Grote W, et al. Eur J Pediatr. 1983 Mar;140(1):63-6. doi: 10.1007/BF00661909. Eur J Pediatr. 1983. PMID: 6873115

10

Detection of deletions in the short arm of chromosome 3 in uncultured renal cell carcinomas by interphase cytogenetics.

Siebert R, Jacobi C, Matthiesen P, Zühlke-Jenisch R, Potratz C, Zhang Y, Stöckle M, Klöppel G, Grote W, Schlegelberger B. Siebert R, et al. Among authors: grote w. J Urol. 1998 Aug;160(2):534-9. J Urol. 1998. PMID: 9679924

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