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

Year Number of Results
1978 1
1986 1
1988 1
1989 1
1990 1
1992 1
1993 3
1997 4
1998 1
1999 1
2000 4
2002 1
2003 3
2004 1
2005 4
2006 2
2023 0
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29 results
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Page 1
Paracentric inversion inv(11)(q21q23) in The Netherlands.
Madan K, Pieters MH, Kuyt LP, van Asperen CJ, de Pater JM, Hamers AJ, Gerssen-Schoorl KB, Hustinx TW, Breed AS, Van Hemel JO, et al. Madan K, et al. Among authors: de pater jm. Hum Genet. 1990 Jun;85(1):15-20. doi: 10.1007/BF00276319. Hum Genet. 1990. PMID: 2358301
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: de pater jm. Am J Hum Genet. 1993 Feb;52(2):249-54. Am J Hum Genet. 1993. PMID: 8430691 Free PMC article.
Trisomy 8 in chorionic villi-unpredictable results in follow-up.
de Pater JM, Schuring-Blom GH, Nieste-Otter MA, van Nesselrooij B, Kapitein B, Christiaens GC, Leschot NJ. de Pater JM, et al. Prenat Diagn. 2000 May;20(5):435-7. doi: 10.1002/(sici)1097-0223(200005)20:5<435::aid-pd823>;2-q. Prenat Diagn. 2000. PMID: 10820417 No abstract available.
A third case of de novo partial trisomy 4p.
Oorthuys JW, Gerssen-Schoorl KB, de Pater JM, de France HF. Oorthuys JW, et al. Among authors: de pater jm. J Med Genet. 1989 May;26(5):344-5. doi: 10.1136/jmg.26.5.344. J Med Genet. 1989. PMID: 2732997 Free PMC article. No abstract available.
29 results