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Table representation of search results timeline featuring number of search results per year.

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

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77 results

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Page 1
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.
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.
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
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.
77 results