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Items: 1 to 20 of 146

1.

Are all cases of low-grade mosaic trisomy 13 in amniotic fluid with no fetal malformation in fact confined placental mosaicism? A case report.

Etoubleau C, Bourthoumieu S, Fiorenza M, Aubard V, Yardin C.

Morphologie. 2011 Dec;95(311):142-5. doi: 10.1016/j.morpho.2011.07.117. Epub 2011 Nov 10.

PMID:
22079601
2.

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.

PMID:
8734806
3.

Positive cell-free fetal DNA testing for trisomy 13 reveals confined placental mosaicism.

Hall AL, Drendel HM, Verbrugge JL, Reese AM, Schumacher KL, Griffith CB, Weaver DD, Abernathy MP, Litton CG, Vance GH.

Genet Med. 2013 Sep;15(9):729-32. doi: 10.1038/gim.2013.26. Epub 2013 Mar 14.

PMID:
23492874
5.

Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.

Hsu LY, Yu MT, Neu RL, Van Dyke DL, Benn PA, Bradshaw CL, Shaffer LG, Higgins RR, Khodr GS, Morton CC, Wang H, Brothman AR, Chadwick D, Disteche CM, Jenkins LS, Kalousek DK, Pantzar TJ, Wyatt P.

Prenat Diagn. 1997 Mar;17(3):201-42.

PMID:
9110367
6.

Placental mosaicism for Trisomy 13: a challenge in providing the cell-free fetal DNA testing.

Liu XY, Zhang HG, Wang RX, Chen S, Yu XW, Liu RZ.

J Assist Reprod Genet. 2014 May;31(5):589-94. doi: 10.1007/s10815-014-0182-7. Epub 2014 Feb 5.

7.

Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies.

Genuardi M, Tozzi C, Pomponi MG, Stagni ML, Della Monica M, Scarano G, Calvieri F, Torrisi L, Neri G.

Eur J Hum Genet. 1999 May-Jun;7(4):421-6.

8.

Prenatal diagnosis of trisomy 3 mosaicism.

Zaslav AL, Pierno G, Davis J, Fougner A, Jacob J, Kazi R, Blumenthal D, Sturim S, Shaham M, Fox J.

Prenat Diagn. 2004 Sep;24(9):693-6. Review.

PMID:
15386452
9.

Postnatal confirmation of prenatally diagnosed trisomy 16 mosaicism in two phenotypically abnormal liveborns.

Pletcher BA, Sanz MM, Schlessel JS, Kunaporn S, McKenna C, Bialer MG, Alonso ML, Zaslav AL, Brown WT, Ray JH.

Prenat Diagn. 1994 Oct;14(10):933-40.

PMID:
7899268
10.

Outcome of prenatally diagnosed trisomy 6 mosaicism.

Wallerstein R, Oh T, Durcan J, Abdelhak Y, Clachko M, Aviv H.

Prenat Diagn. 2002 Aug;22(8):722-4.

PMID:
12210584
11.

Uniparental disomy for chromosome 16 in humans.

Kalousek DK, Langlois S, Barrett I, Yam I, Wilson DR, Howard-Peebles PN, Johnson MP, Giorgiutti E.

Am J Hum Genet. 1993 Jan;52(1):8-16.

12.

Non-mosaic trisomy 20 of paternal origin in chorionic villus and amniotic fluid also detected in fetal blood and other tissues.

Morales C, Cuatrecasas E, Mademont-Soler I, Clusellas N, Peruga E, Català V, Garrido C, Milà M, Soler A, Sánchez A.

Eur J Med Genet. 2010 Jul-Aug;53(4):197-200. doi: 10.1016/j.ejmg.2010.03.007. Epub 2010 Mar 27.

PMID:
20350623
13.

Sonographically detected fetal and placental abnormalities associated with trisomy 16 confined to the placenta. A case report and review of the literature.

Astner A, Schwinger E, Caliebe A, Jonat W, Gembruch U.

Prenat Diagn. 1998 Dec;18(12):1308-15. Review.

PMID:
9885025
14.

Normal outcome of a pregnancy with mosaicism for double trisomy in amniotic fluid cells.

Bartels I, Franke U, Braulke I, Rauskolb R, Raab-Vetter M.

Prenat Diagn. 1997 Sep;17(9):877-8.

PMID:
9316135
15.

Prospective prenatal investigations on potential uniparental disomy in cases of confined placental trisomy.

Van Opstal D, Van den Berg C, Deelen WH, Brandenburg H, Cohen-Overbeek TE, Halley DJ, Van den Ouweland AM, In 't Veld PA, Los FJ.

Prenat Diagn. 1998 Jan;18(1):35-44.

PMID:
9483638
16.

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.

PMID:
8606880
17.

Trisomy 16 mosaicism in amniotic fluid cell cultures.

Tantravahi U, Matsumoto C, Delach J, Craffey A, Smeltzer J, Benn P.

Prenat Diagn. 1996 Aug;16(8):749-54.

PMID:
8878286
18.

Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell- Silver syndrome.

Petit F, Holder-Espinasse M, Duban-Bedu B, Bouquillon S, Boute-Benejean O, Bazin A, Rouland V, Manouvrier-Hanu S, Delobel B.

Clin Genet. 2012 Mar;81(3):265-71. doi: 10.1111/j.1399-0004.2010.01621.x. Epub 2011 Jan 19.

PMID:
21204802
19.

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.

PMID:
8938058
20.

[Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].

Ulmer R, Pfeiffer RA, Kollert A, Beinder E.

Z Geburtshilfe Neonatol. 2000 Jan-Feb;204(1):1-7. German.

PMID:
10721179
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