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Showing results for pater jm
Search for Paer JMP instead (1 results)
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
Misleading variant chromosome 12 in prenatal diagnosis.
de Pater JM, Brocker-Vriends AH, Verschuren M, Linders DA, Hansson KB. de Pater JM, et al. Prenat Diagn. 2006 Jun;26(6):587-8. doi: 10.1002/pd.1464. Prenat Diagn. 2006. PMID: 16739240 No abstract available.
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.
56 results