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Clinical aspects, prenatal diagnosis, and pathogenesis of trisomy 16 mosaicism.
Yong PJ, Barrett IJ, Kalousek DK, Robinson WP. Yong PJ, et al. Among authors: robinson wp. J Med Genet. 2003 Mar;40(3):175-82. doi: 10.1136/jmg.40.3.175. J Med Genet. 2003. PMID: 12624135 Free PMC article.
Sex-specific meiotic recombination in the Prader--Willi/Angelman syndrome imprinted region.
Robinson WP, Lalande M. Robinson WP, et al. Hum Mol Genet. 1995 May;4(5):801-6. doi: 10.1093/hmg/4.5.801. Hum Mol Genet. 1995. PMID: 7633438
Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection.
Robinson WP, Binkert F, Bernasconi F, Lorda-Sanchez I, Werder EA, Schinzel AA. Robinson WP, et al. Am J Hum Genet. 1995 Feb;56(2):444-51. Am J Hum Genet. 1995. PMID: 7847381 Free PMC article.
Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?
Bottani A, Robinson WP, DeLozier-Blanchet CD, Engel E, Morris MA, Schmitt B, Thun-Hohenstein L, Schinzel A. Bottani A, et al. Among authors: robinson wp. Am J Med Genet. 1994 May 15;51(1):35-40. doi: 10.1002/ajmg.1320510109. Am J Med Genet. 1994. PMID: 8030667
Parental origin of the supernumerary chromosome in trisomy 18.
Ya-gang X, Robinson WP, Spiegel R, Binkert F, Ruefenacht U, Schinzel AA. Ya-gang X, et al. Among authors: robinson wp. Clin Genet. 1993 Aug;44(2):57-61. doi: 10.1111/j.1399-0004.1993.tb03847.x. Clin Genet. 1993. PMID: 8275560
Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.
Robinson WP, Wagstaff J, Bernasconi F, Baccichetti C, Artifoni L, Franzoni E, Suslak L, Shih LY, Aviv H, Schinzel AA. Robinson WP, et al. J Med Genet. 1993 Sep;30(9):756-60. doi: 10.1136/jmg.30.9.756. J Med Genet. 1993. PMID: 8411071 Free PMC article.
Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion.
Robinson WP, Waslynka J, Bernasconi F, Wang M, Clark S, Kotzot D, Schinzel A. Robinson WP, et al. Genomics. 1996 May 15;34(1):17-23. doi: 10.1006/geno.1996.0237. Genomics. 1996. PMID: 8661020
Molecular studies of translocations and trisomy involving chromosome 13.
Robinson WP, Bernasconi F, Dutly F, Lefort G, Romain DR, Binkert F, Schinzel AA. Robinson WP, et al. Am J Med Genet. 1996 Jan 11;61(2):158-63. doi: 10.1002/(SICI)1096-8628(19960111)61:2<158::AID-AJMG11>3.0.CO;2-T. Am J Med Genet. 1996. PMID: 8669444
Mosaicism most likely accounts for extended survival of trisomy 22.
Robinson WP, Kalousek DK. Robinson WP, et al. Am J Med Genet. 1996 Mar 1;62(1):100-1. doi: 10.1002/(SICI)1096-8628(19960301)62:1<100::AID-AJMG21>3.0.CO;2-V. Am J Med Genet. 1996. PMID: 8779317 No abstract available.
Kallmann syndrome in a boy with a t(1;10) translocation detected by reverse chromosome painting.
Schinzel A, Lorda-Sanchez I, Binkert F, Carter NP, Bebb CE, Ferguson-Smith MA, Eiholzer U, Zachmann M, Robinson WP. Schinzel A, et al. Among authors: robinson wp. J Med Genet. 1995 Dec;32(12):957-61. doi: 10.1136/jmg.32.12.957. J Med Genet. 1995. PMID: 8825924 Free PMC article.
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