Beverstock G[au] - Search Results

Year	Number of Results
1981	2
1982	2
1983	1
1984	3
1985	1
1986	3
1987	6
1988	4
1989	5
1990	7
1991	11
1992	5
1993	6
1994	1
1995	4
1996	5
1997	6
1998	5
1999	2
2000	2
2002	1
2003	1
2004	1
2022	0

1

De novo acute B-cell leukemia with translocation t(14;18): an entity with a poor prognosis.

Kramer MH, Raghoebier S, Beverstock GC, de Jong D, Kluin PM, Kluin-Nelemans JC. Kramer MH, et al. Among authors: beverstock gc. Leukemia. 1991 Jun;5(6):473-8. Leukemia. 1991. PMID: 1711639 Review.

2

Y chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile male.

Beverstock GC, MacFarlane JD, Veenema H, Hoekman H, Goodfellow PJ. Beverstock GC, et al. J Med Genet. 1989 May;26(5):330-3. doi: 10.1136/jmg.26.5.330. J Med Genet. 1989. PMID: 2659792 Free PMC article. Review.

3

Nasopharyngeal teratoma and mosaic tetrasomy 1q detected at amniocentesis. A case report and review of the literature.

Beverstock GC, Mollevanger P, Baaij M, Lind J, van Ieperen L, Bartelings MM, Teunissen K, Brandenburg H, Van Opstal D, Los F. Beverstock GC, et al. Cancer Genet Cytogenet. 1999 Nov;115(1):11-8. doi: 10.1016/s0165-4608(99)00084-9. Cancer Genet Cytogenet. 1999. PMID: 10565293 Review.

4

The current state of research with peripheral tissues in Huntington disease.

Beverstock GC. Beverstock GC. Hum Genet. 1984;66(2-3):115-31. doi: 10.1007/BF00286586. Hum Genet. 1984. PMID: 6325322 Review.

5

t(5;12)(q31;p12). A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia.

Wessels JW, Fibbe WE, van der Keur D, Landegent JE, van der Plas DC, den Ottolander GJ, Roozendaal KJ, Beverstock GC. Wessels JW, et al. Among authors: beverstock gc. Cancer Genet Cytogenet. 1993 Jan;65(1):7-11. doi: 10.1016/0165-4608(93)90051-m. Cancer Genet Cytogenet. 1993. PMID: 8431918 Review.

6

A girl with 71,XXXXY karyotype.

Maaswinkel-Mooij PD, van Zwieten P, Mollevanger P, van Noort E, Beverstock G. Maaswinkel-Mooij PD, et al. Among authors: beverstock g. Clin Genet. 1992 Feb;41(2):96-9. doi: 10.1111/j.1399-0004.1992.tb03641.x. Clin Genet. 1992. PMID: 1544219

7

Trisomy 13 and myelodysplastic syndrome.

Beverstock GC, Ploem JE, Wessels H, van de Keur D, Mollevanger P. Beverstock GC, et al. Cancer Genet Cytogenet. 1990 Sep;48(2):179-82. doi: 10.1016/0165-4608(90)90117-s. Cancer Genet Cytogenet. 1990. PMID: 2397449

8

Detection of the Philadelphia chromosome in interphase nuclei.

Arnoldus EP, Wiegant J, Noordermeer IA, Wessels JW, Beverstock GC, Grosveld GC, van der Ploeg M, Raap AK. Arnoldus EP, et al. Among authors: beverstock gc. Cytogenet Cell Genet. 1990;54(3-4):108-11. doi: 10.1159/000132972. Cytogenet Cell Genet. 1990. PMID: 2265553

9

Monosomy 8p: an easily overlooked syndrome.

Bröcker-Vriends AH, Mooij PD, van Bel F, Beverstock GC, van de Kamp JJ. Bröcker-Vriends AH, et al. Among authors: beverstock gc. J Med Genet. 1986 Apr;23(2):153-4. doi: 10.1136/jmg.23.2.153. J Med Genet. 1986. PMID: 3712390 Free PMC article.

10

Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3.

Breuning MH, Dauwerse HG, Fugazza G, Saris JJ, Spruit L, Wijnen H, Tommerup N, van der Hagen CB, Imaizumi K, Kuroki Y, van den Boogaard MJ, de Pater JM, Mariman EC, Hamel BC, Himmelbauer H, Frischauf AM, Stallings R, Beverstock GC, van Ommen GJ, Hennekam RC. Breuning MH, et al. Among authors: beverstock gc. Am J Hum Genet. 1993 Feb;52(2):249-54. Am J Hum Genet. 1993. PMID: 8430691 Free PMC article.

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