Warning: The NCBI web site requires JavaScript to function. more...
On the paternal origin of trisomy 21 Down syndrome.
Hultén MA, Patel SD, Westgren M, Papadogiannakis N, Jonsson AM, Jonasson J, Iwarsson E.
Mol Cytogenet. 2010 Feb 23;3:4.
Related citations
On the origin of trisomy 21 Down syndrome.
Hultén MA, Patel SD, Tankimanova M, Westgren M, Papadogiannakis N, Jonsson AM, Iwarsson E.
Mol Cytogenet. 2008 Sep 18;1:21.
Final Report on Carcinogens Background Document for Formaldehyde.
National Toxicology Program.
Rep Carcinog Backgr Doc. 2010 Jan;(10-5981):i-512.
Final Report on Carcinogens Background Document for Styrene.
Rep Carcinog Backgr Doc. 2008 Sep;(8-5978):i-398.
Germ-line transmission of trisomy 21: Data from 80 families suggest an implication of grandmaternal age and a high frequency of female-specific trisomy rescue.
Kovaleva NV.
Mol Cytogenet. 2010 Mar 18;3:7.
Down syndrome: a study of chromosomal mosaicism.
Modi D, Berde P, Bhartiya D.
Reprod Biomed Online. 2003 Jun;6(4):499-503.
Comparison of modes of ascertainment for mosaic vs complete trisomy 21.
Bornstein E, Lenchner E, Donnenfeld A, Kapp S, Keeler SM, Divon MY.
Am J Obstet Gynecol. 2009 Apr;200(4):440.e1-5.
Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism.
Christian SL, Smith AC, Macha M, Black SH, Elder FF, Johnson JM, Resta RG, Surti U, Suslak L, Verp MS, Ledbetter DH.
Prenat Diagn. 1996 Apr;16(4):323-32.
Periodic health examination, 1996 update: 1. Prenatal screening for and diagnosis of Down syndrome. Canadian Task Force on the Periodic Health Examination.
Dick PT.
CMAJ. 1996 Feb 15;154(4):465-79.
Non-mosaic trisomy 16 in a third-trimester fetus.
Yancey MK, Hardin EL, Pacheco C, Kuslich CD, Donlon TA.
Obstet Gynecol. 1996 May;87(5 Pt 2):856-60.
Mosaicism for trisomy 12: four cases with varying outcomes.
Bischoff FZ, Zenger-Hain J, Moses D, Van Dyke DL, Shaffer LG.
Prenat Diagn. 1995 Nov;15(11):1017-26.
Karyotype, phenotype and parental origin in 19 cases of triploidy.
Daniel A, Wu Z, Bennetts B, Slater H, Osborn R, Jackson J, Pupko V, Nelson J, Watson G, Cooke-Yarborough C, Loo C.
Prenat Diagn. 2001 Dec;21(12):1034-48.
A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error.
Chen CP, Chern SR, Tsai FJ, Lin CY, Lin YH, Wang W.
Prenat Diagn. 2005 Apr;25(4):327-30.
[Sex ratio in Down syndrome].
Tsitol Genet. 2002 Nov-Dec;36(6):54-69. Review. Russian.
Parental origin of the extra chromosome in prenatally diagnosed fetal trisomy 21.
Muller F, Rebiffé M, Taillandier A, Oury JF, Mornet E.
Hum Genet. 2000 Mar;106(3):340-4.
Recurrent trisomy 21: four cases in three generations.
Gair JL, Arbour L, Rupps R, Jiang R, Bruyère H, Robinson WP.
Clin Genet. 2005 Nov;68(5):430-5.
Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line.
Bruyère H, Rupps R, Kuchinka BD, Friedman JM, Robinson WP.
Am J Med Genet. 2000 Sep 4;94(1):35-41.
Cytogenetic analysis of chorionic villi for prenatal diagnosis: an ACC collaborative study of U.K. data. Association of Clinical Cytogeneticists Working Party on Chorionic Villi in Prenatal Diagnosis.
[No authors listed]
Prenat Diagn. 1994 May;14(5):363-79.
Analysis of nine pregnancies with confined placental mosaicism for trisomy 2.
Shaffer LG, Langlois S, McCaskill C, Main DM, Robinson WP, Barrett IJ, Kalousek DK.
Prenat Diagn. 1996 Oct;16(10):899-905.
[Chromosome 21 mosaicism. A review].
Tsitologiia. 2003;45(4):434-40. Review. Russian.
Filter your results:
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on