Kalousek DK - Search Results

1

Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies.

Beever CL, Stephenson MD, Peñaherrera MS, Jiang RH, Kalousek DK, Hayden M, Field L, Brown CJ, Robinson WP. Beever CL, et al. Among authors: kalousek dk. Am J Hum Genet. 2003 Feb;72(2):399-407. doi: 10.1086/346119. Epub 2002 Dec 20. Am J Hum Genet. 2003. PMID: 12497247 Free PMC article.

2

Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction.

Robinson WP, Barrett IJ, Bernard L, Telenius A, Bernasconi F, Wilson RD, Best RG, Howard-Peebles PN, Langlois S, Kalousek DK. Robinson WP, et al. Among authors: kalousek dk. Am J Hum Genet. 1997 Apr;60(4):917-27. Am J Hum Genet. 1997. PMID: 9106539 Free PMC article.

3

Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism.

Lau AW, Brown CJ, Peñaherrera M, Langlois S, Kalousek DK, Robinson WP. Lau AW, et al. Among authors: kalousek dk. Am J Hum Genet. 1997 Dec;61(6):1353-61. doi: 10.1086/301651. Am J Hum Genet. 1997. PMID: 9399909 Free PMC article.

4

An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta.

Peñaherrera MS, Barrett IJ, Brown CJ, Langlois S, Yong SL, Lewis S, Bruyère H, Howard-Peebles PN, Kalousek DK, Robinson WP. Peñaherrera MS, et al. Among authors: kalousek dk. Clin Genet. 2000 Dec;58(6):436-46. doi: 10.1034/j.1399-0004.2000.580603.x. Clin Genet. 2000. PMID: 11149612

5

Evidence for imprinting on chromosome 16: the effect of uniparental disomy on the outcome of mosaic trisomy 16 pregnancies.

Yong PJ, Marion SA, Barrett IJ, Kalousek DK, Robinson WP. Yong PJ, et al. Among authors: kalousek dk. Am J Med Genet. 2002 Oct 1;112(2):123-32. doi: 10.1002/ajmg.10702. Am J Med Genet. 2002. PMID: 12244544

6

Clinical aspects, prenatal diagnosis, and pathogenesis of trisomy 16 mosaicism.

Yong PJ, Barrett IJ, Kalousek DK, Robinson WP. Yong PJ, et al. Among authors: kalousek dk. 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.

7

Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss.

Rajcan-Separovic E, Diego-Alvarez D, Robinson WP, Tyson C, Qiao Y, Harvard C, Fawcett C, Kalousek D, Philipp T, Somerville MJ, Stephenson MD. Rajcan-Separovic E, et al. Hum Reprod. 2010 Nov;25(11):2913-22. doi: 10.1093/humrep/deq202. Epub 2010 Sep 16. Hum Reprod. 2010. PMID: 20847186

8

Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism.

Robinson WP, McFadden DE, Barrett IJ, Kuchinka B, Peñaherrera MS, Bruyère H, Best RG, Pedreira DA, Langlois S, Kalousek DK. Robinson WP, et al. Among authors: kalousek dk. Prenat Diagn. 2002 Dec;22(12):1076-85. doi: 10.1002/pd.483. Prenat Diagn. 2002. PMID: 12454962

9

Placental weight in pregnancies with trisomy confined to the placenta.

Yong PJ, von Dadelszen P, McFadden DE, Barrett IJ, Kalousek DK, Robinson WP. Yong PJ, et al. Among authors: kalousek dk. J Obstet Gynaecol Can. 2009 Jul;31(7):605-610. doi: 10.1016/S1701-2163(16)34239-6. J Obstet Gynaecol Can. 2009. PMID: 19761633

10

Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases.

Kalousek DK, Langlois S, Robinson WP, Telenius A, Bernard L, Barrett IJ, Howard-Peebles PN, Wilson RD. Kalousek DK, et al. Am J Med Genet. 1996 Nov 11;65(4):348-52. doi: 10.1002/(SICI)1096-8628(19961111)65:4<348::AID-AJMG19>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8923948

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