Beverstock GC[au] - Search Results

Year	Number of Results
1981	2
1982	2
1983	1
1984	3
1985	1
1986	3
1987	5
1988	4
1989	5
1990	7
1991	10
1992	4
1993	6
1994	1
1995	3
1996	3
1997	6
1998	4
1999	2
2000	2
2002	1
2003	1
2004	1
2023	0

1

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.

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

A second case of hexasomy 8 in myelodysplastic syndrome.

Beverstock GC, Wessels HW, Mollevanger P, den Ottolander GJ, Gottlieb DJ. Beverstock GC, et al. Cancer Genet Cytogenet. 1997 Nov;99(1):68-72. doi: 10.1016/s0165-4608(96)00441-4. Cancer Genet Cytogenet. 1997. PMID: 9352798 Review.

4

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.

5

Multiple supernumerary ring chromosomes of different origin in a patient: a clinical report and review of the literature.

Beverstock GC, Bezrookove V, Mollevanger P, van de Kamp JJ, Pearson P, Kouwenberg JM, Rosenberg C. Beverstock GC, et al. Am J Med Genet A. 2003 Oct 1;122A(2):168-73. doi: 10.1002/ajmg.a.20163. Am J Med Genet A. 2003. PMID: 12955771 Review.

6

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.

7

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.

8

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.

9

A patient with dup(10p)del(8q) and Pendred syndrome.

van Wouwe JP, Wijnands MC, Mourad-Baars PE, Geraedts JP, Beverstock GC, van de Kamp JJ. van Wouwe JP, et al. Among authors: beverstock gc. Am J Med Genet. 1986 Jun;24(2):211-7. doi: 10.1002/ajmg.1320240202. Am J Med Genet. 1986. PMID: 3717206

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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